Label: ALBUTEROL SULFATE solution

Albuterol sulfate inhalation solution is a sterile, clear, colorless solution of the sulfate salt of racemic albuterol, albuterol sulfate. Albuterol sulfate is a relatively selective beta 2-adrenergic bronchodilator (see CLINICAL PHARMACOLOGY). The chemical name for albuterol sulfate is α 1 [(tert-butylamino) methyl]-4-hydroxy-m-­xylene-α,α’-diol sulfate (2:1) (salt), and its established chemical structure is as follows:



The molecular weight of albuterol sulfate is 576.7 and the molecular formula is (C 13H 21NO 3) 2• H 2SO 4. Albuterol sulfate USP is a white or practically white powder, freely soluble in water, slightly soluble in alcohol, in ether and practically insoluble in chloroform. The World Health Organization recommended name for albuterol is salbutamol.

Albuterol sulfate inhalation solution is supplied in two strengths in unit dose vials. Each unit dose vial contains either 0.63 mg of albuterol equivalent to 0.75 mg of albuterol sulfate or 1.25 mg of albuterol equivalent to 1.5 mg of albuterol sulfate with sodium chloride and sulfuric acid in a 3-mL isotonic, sterile, aqueous solution. Sodium chloride is added to adjust isotonicity of the solution and sulfuric acid is added to adjust pH of the solution to 3.5 (see HOW SUPPLIED).

Albuterol sulfate inhalation solution does not require dilution prior to administration by nebulization. For albuterol sulfate inhalation solution, like all other nebulized treatments, the amount delivered to the lungs will depend on patient factors, the jet nebulizer utilized, and compressor performance. Using the Pari LC Plus TM nebulizer (with face mask or mouthpiece) connected to a Pari PRONEB TM compressor, under in vitro conditions, the mean delivered dose from the mouth piece (% nominal dose) was approximately 43% of albuterol (1.25 mg strength) and 39% of albuterol (0.63 mg strength) at a mean flow rate of 3.6 L/min. The mean nebulization time was 15 minutes or less. Albuterol sulfate inhalation solution should be administered from a jet nebulizer at an adequate flow rate, via a mouthpiece or face mask (see DOSAGE AND ADMINISTRATION).

The prime action of beta-adrenergic drugs is to stimulate adenyl cyclase, the enzyme which catalyzes the formation of cyclic-3',5'-adenosine monophosphate (cyclic AMP) from adenosine triphosphate (ATP). The cyclic AMP thus formed mediates the cellular responses. In vitro studies and in vivo pharmacologic studies have demonstrated that albuterol has a preferential effect on beta 2-adrenergic receptors compared with isoproterenol. While it is recognized that beta 2-adrenergic receptors are the predominant receptors in bronchial smooth muscle, recent data indicate that 10% to 50% of the beta- receptors in the human heart may be beta 2-receptors. The precise function of these receptors, however, is not yet established. Controlled clinical studies and other clinical experience have shown that inhaled albuterol, like other beta-adrenergic agonist drugs, can produce a significant cardiovascular effect in some patients, as measured by pulse rate, blood pressure, symptoms, and/or electrocardiographic changes. Albuterol is longer acting than isoproterenol in most patients by any route of administration because it is not a substrate for the cellular uptake processes for catecholamines nor for catechol-O-methyl transferase.

Pharmacokinetics:Studies in asthmatic patients have shown that less than 20% of a single albuterol dose was absorbed following either intermittent positive-pressure breathing (IPPB) or nebulizer administration; the remaining amount was recovered from the nebulizer and apparatus, and expired air. Most of the absorbed dose was recovered in urine collected during the 24 hours after drug administration. Following oral administration of 4 mg albuterol, the elimination half-life was five to six hours. Following a 3 mg dose of nebulized albuterol in adults, the mean maximum albuterol plasma level at 0.5 hours was 2.1 ng/mL (range, 1.4 to 3.2 ng/mL). The pharmacokinetics of albuterol following administration of 0.63 mg or 1.25 mg albuterol sulfate inhalation solution by nebulization have not been determined in children 2 to 12 years old.

Animal Pharmacology/Toxicology:Intravenous studies in rats with albuterol sulfate have demonstrated that albuterol crosses the blood-brain barrier and reaches brain concentrations amounting to approximately 5% of plasma concentrations. In structures outside the blood-brain barrier (pineal and pituitary glands), albuterol concentrations were found to be 100 times those found in whole brain.

Studies in laboratory animals (minipigs, rodents, and dogs) have demonstrated the occurrence of cardiac arrhythmias and sudden death (with histologic evidence of myocardial necrosis) when beta-agonists and methylxanthines are administered concurrently. The clinical significance of these findings is unknown.

Clinical Trials:The safety and efficacy of albuterol sulfate inhalation solution was evaluated in a 4-week, multi­-center, randomized, double-blind, placebo-controlled, parallel group study in 349 children 6 to 12 years of age with mild-to-moderate asthma (mean baseline FEV 1 60% to 70% of predicted). Approximately half of the patients were also receiving inhaled corticosteroids. Patients were randomized to receive albuterol sulfate inhalation solution 0.63 mg, albuterol sulfate inhalation solution 1.25 mg, or placebo three times a day administered via a Pari LC Plus TM nebulizer and a Pari PRONEB TM compressor. Racemic albuterol, delivered by a chlorofluorocarbon (CFC) metered dose inhaler (MDI) or nebulized, was used on an as-needed basis as the rescue medication.

Efficacy, as measured by the mean percent change from baseline in the area under the 6­-hour curve for FEV 1, was demonstrated for both active treatment regimens (n=112 [1.25 mg group] and n=110 [0.63 mg group]) compared with placebo (n=110) on day 1 and day 28. Figures 1 and 2 illustrate the mean percentage change from pre-dose FEV 1 on day 1 and day 28, respectively. The mean baseline FEV 1 for all patients was 1.49 L.

The onset of a 15% increase in FEV 1 over baseline for both doses of albuterol sulfate inhalation solution was seen at 30 minutes (the first post-dose assessment). The mean time to peak effect was approximately 30 to 60 minutes for both doses on day 1 and after 4 weeks of treatment. The mean duration of effect, as measured by a >15% increase from baseline in FEV 1, was approximately 2.5 hours for both doses on day 1 and approximately 2 hours for both doses after 4 weeks of treatment. In some patients, the duration of effect was as long as 6 hours.

Albuterol sulfate inhalation solution is indicated for the relief of bronchospasm in patients 2 to 12 years of age with asthma (reversible obstructive airway disease).

Albuterol sulfate inhalation solution is contraindicated in patients with a history of hypersensitivity to any of its components.

Paradoxical Bronchospasm:As with other inhaled beta-adrenergic agonists, albuterol sulfate inhalation solution can produce paradoxical bronchospasm, which may be life threatening. If paradoxical bronchospasm occurs, albuterol sulfate inhalation solution should be discontinued immediately and alternative therapy instituted. It should be noted that paradoxical bronchospasm, when associated with inhaled formulations, frequently occurs with the first use of a new canister or vial.

Use of Anti-Inflammatory Agents: The use of beta-adrenergic bronchodilators alone may not be adequate to control asthma in many patients. Early consideration should be given to adding anti-inflammatory agents (e.g., corticosteroids).

Deterioration of Asthma:Asthma may deteriorate acutely over a period of hours or chronically over several days or longer. If the patient needs more doses of albuterol sulfate inhalation solution than usual, this may be a marker of destabilization of asthma and requires re-evaluation of the patient and the treatment regimen, giving special consideration of the possible need for anti-inflammatory treatment (e.g., corticosteroids).

Fatalities have been reported in association with excessive use of inhaled sympathomimetic drugs and with the home use of nebulizers. It is, therefore, essential that the physician instruct the patient in the need for further evaluation, if his/her asthma becomes worse.

Cardiovascular Effects:Albuterol sulfate inhalation solution, like other beta-adrenergic agonists, can produce a clinically significant cardiovascular effect in some patients as measured by pulse rate, blood pressure, and/or symptoms. Although such effects are uncommon for albuterol sulfate inhalation solution at recommended doses, if they occur, the drug may need to be discontinued. In addition, beta-agonists have been reported to produce ECG changes, such as flattening of the T- wave, prolongation of the QTc interval, and ST segment depression. The clinical significance of these findings is unknown. Therefore, albuterol sulfate inhalation solution like all other sympathomimetic amines, should be used with caution in patients with cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, and hypertension.

Immediate Hypersensitivity Reactions:Immediate hypersensitivity reactions may occur after administration of albuterol as demonstrated by rare cases of urticaria, angioedema, rash, bronchospasm, and oropharyngeal edema.

Clinical Trial Experience: Adverse events reported in >1% of patients receiving albuterol sulfate inhalation solution and more frequently than in patients receiving placebo in a four-week double- blind study are listed in the following table.

There was one case of ST segment depression in the 1.25 mg albuterol sulfate inhalation solution treatment group.



No clinically relevant laboratory abnormalities related to albuterol sulfate inhalation solution administration were seen in this study.



Postmarketing Experience: Metabolic acidosis has been reported after the use of albuterol sulfate inhalation solution. Because this reaction is reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate its frequency or establish a causal relationship to drug exposure.

The expected symptoms with overdosage are those of excessive beta-adrenergic stimulation and/or occurrence or exaggeration of symptoms such as seizures, angina, hypertension or hypotension, tachycardia with rates up to 200 beats per minute, arrhythmias, nervousness, headache, tremor, dry mouth, palpitation, nausea, dizziness, fatigue, malaise, insomnia, and exaggeration of the pharmacological effects listed in ADVERSE REACTIONS. Hypokalemia may also occur. As with all sympathomimetic aerosol medications, cardiac arrest and even death may be associated with abuse of albuterol sulfate inhalation solution. Treatment consists of discontinuation of albuterol sulfate inhalation solution together with appropriate symptomatic therapy. The judicious use of a cardioselective beta-receptor blocker may be considered, bearing in mind that such medication can produce bronchospasm. There is insufficient evidence to determine if dialysis is beneficial for overdosage of albuterol sulfate inhalation solution.

The oral median lethal dose of albuterol sulfate in mice is greater than 2,000 mg/kg (approximately 580 times the maximum recommended daily inhalation dose of albuterol sulfate inhalation solution on a mg/m 2 basis). The subcutaneous median lethal dose of albuterol sulfate in mature rats and small young rats is approximately 450 mg/kg and 2,000 mg/kg, respectively (approximately 260 and 1,200 times the maximum recommended daily inhalation dose of albuterol sulfate inhalation solution on a mg/m 2 basis). The inhalation median lethal dose has not been determined in animals.

The usual starting dosage for patients 2 to 12 years of age is 1.25 mg or 0.63 mg of albuterol sulfate inhalation solution administered 3 or 4 times daily, as needed, by nebulization. More frequent administration is not recommended.

To administer 1.25 mg or 0.63 mg of albuterol, use the entire contents of one unit-dose vial (3 mL of 1.25 mg or 0.63 mg inhalation solution) by nebulization. Adjust nebulizer flow rate to deliver albuterol sulfate inhalation solution over 5 to 15 minutes.

The use of albuterol sulfate inhalation solution can be continued as medically indicated to control recurring bouts of bronchospasm. During this time most patients gain optimum benefit from regular use of the inhalation solution.

Patients 6 to 12 years of age with more severe asthma (baseline FEV 1 less than 60% predicted), weight >40 kg, or patients 11 to 12 years of age may achieve a better initial response with the 1.25 mg dose.

Albuterol sulfate inhalation solution has not been studied in the setting of acute attacks of bronchospasm. A 2.5 mg dose of albuterol provided by a higher concentration product (2.5 mg albuterol per 3 mL) may be more appropriate for treating acute exacerbations, particularly in children 6 years old and above.

If a previously effective dosage regimen fails to provide the usual relief, medical advice should be sought immediately, as this is often a sign of seriously worsening asthma which would require reassessment of therapy.

The drug compatibility (physical and chemical), clinical efficacy and safety of albuterol sulfate inhalation solution, when mixed with other drugs in a nebulizer have not been established.

The safety and efficacy of albuterol sulfate inhalation solution have been established in clinical trials when administered using the Pari LC Plus TM nebulizer and Pari PRONEB TM compressor. The safety and efficacy of albuterol sulfate inhalation solution when administered with other nebulizer systems have not been established.

Albuterol sulfate inhalation solution should be administered via jet nebulizer connected to an air compressor with adequate air flow, equipped with a mouthpiece or suitable face mask.

Albuterol Sulfate Inhalation Solution is supplied as a 3 mL, clear, colorless, sterile, preservative-free, aqueous solution in two different strengths, 0.63 mg/3 mL and 1.25 mg/3 mL, of albuterol (equivalent to 0.75 mg of albuterol sulfate or 1.5 mg of albuterol sulfate per 3 mL) in unit-dose low-density polyethylene (LDPE) vials. Each unit-dose LDPE vial is protected in a foil pouch, and each foil pouch contains 5 unit-dose LDPE vials. Each strength of albuterol sulfate inhalation solution is available in a shelf carton containing multiple foil pouches.



Albuterol Sulfate Inhalation Solution, 0.63 mg/3 mL(potency expressed as albuterol) contains 0.75 mg albuterol sulfate per 3 mL:



Foil pouch of five 3 mL unit-dose vials NDC 81894-105-05

5 such foil pouches in a carton (25 unit-dose vials) NDC 81894-105-25

6 such foil pouches in a carton (30 unit-dose vials) NDC 81894-105-30



Albuterol Sulfate Inhalation Solution, 1.25 mg/3 mL(potency expressed as albuterol) contains 1.50 mg albuterol sulfate per 3 mL:



Foil pouch of five 3 mL unit-dose vials NDC 81894-106-05

5 such foil pouches in a carton (25 unit-dose vials) NDC 81894-106-25

6 such foil pouches in a carton (30 unit-dose vials) NDC 81894-106-30

Store between 2°C to 25°C (36°F to 77°F). Protect from light and excessive heat.



Store unit-dose vials in protective foil pouch at all times. Once removed from the foil pouch, use vial(s) within one week. Discard the vial if the solution is not colorless.



Keep out of the reach of children.



All brands listed are the trademarks of their respective owners and are not trademarks of Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.



Distributed by:

Aurobindo Pharma USA, Inc.

279 Princeton-Hightstown Road

East Windsor, NJ 08520



Manufactured by:

Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.

No.800, Haifa Road, Chengdu Cross-strait Science and Technology Industrial

Development Park, Wenjiang District, Chengdu, Sichuan

China 611130

Revised: July 2024

Albuterol Sulfate Inhalation Solution

(al bue' ter ol sul' fate)

0.63 mg*/3 mL and 1.25 mg*/3 mL

(*Equivalent to 0.75 mg of albuterol sulfate or 1.5 mg of albuterol sulfate per 3 mL)

Read the patient information that comes with albuterol sulfate inhalation solution before using it and each time you get a refill for your child. There may be new information. This leaflet does not take the place of talking to your child's doctor about your child's medical condition or treatment.

What is albuterol sulfate inhalation solution?

Albuterol sulfate inhalation solution is a medicine that is used for the relief of bronchospasms caused by asthma in children ages 2 to 12 years. Bronchospasm is the tightening and swelling of the muscles around the airways. Albuterol sulfate inhalation solution can help relax these airway muscles for up to 6 hours so that your child may breathe more easily.

Who should not use albuterol sulfate inhalation solution?

Do not give your child albuterol sulfate inhalation solution if he or she is allergic to any of its ingredients. The active ingredient is albuterol sulfate. See the end of this leaflet for a complete list of ingredients.

What should I tell my child's doctor before giving albuterol sulfate inhalation solution?

Tell your child's doctor about all of your child's medical conditions including if your child has:

• Heart problems
• High blood pressure
• Seizures
• A thyroid problem called hyperthyroidism
• Diabetes

Tell your child's doctor about all the medicines your child takes, including prescription and non-prescription medicines, vitamins and herbal supplements. Albuterol sulfate inhalation solution and some other medicines can affect each other and may cause serious side effects. Especially tell your child's doctor if your child is taking or using:

• Any short-acting bronchodilator medicines (sometimes called rescue inhalers)
• Epinephrine
• Medicines called monoamine oxidase inhibitors (MAOIs) or tricyclic anti-­depressants or has stopped taking them in the past 2 weeks. These medicines are usually used for mental problems.
• Medicines called beta-blockers (used for heart problems and high blood pressure)
• Certain diuretic medicines (water pills)
• Digoxin

Know the medicines your child takes. Keep a list of them and show it to your child's doctor and pharmacist each time your child gets a new medicine.

How should albuterol sulfate inhalation solution be given?

Read the Patient's Instructions for Use that comes with albuterol sulfate inhalation solution. Ask your pharmacist for these instructions if they are not with your medicine. Keep the instructions with albuterol sulfate inhalation solution because you may want to read them again.

• Give albuterol sulfate inhalation solution exactly as prescribed for your child. Do not change your child's dose or how often it is used without talking to your child's doctor first.
• Albuterol sulfate inhalation solution is breathed into the lungs. Albuterol sulfate inhalation solution is used with a special breathing machine called a nebulizer. Do not mix other medicines with albuterol sulfate inhalation solution in the nebulizer. Do not use albuterol sulfate inhalation solution that is not clear and colorless.
• Call your child's doctor or get emergency help right away if your child's breathing is not helped or gets worse during treatment with albuterol sulfate inhalation solution.
• Call your child's doctor right away if your child needs to use albuterol sulfate inhalation solution more often than prescribed.
• Albuterol sulfate inhalation solution has not been studied for treating acute attacks of bronchospasm (rescue use). Your child may need a different medicine for rescue use.
• If you give your child too much albuterol sulfate inhalation solution, call your child's doctor right away.

What are the side effects with albuterol sulfate inhalation solution?

Albuterol sulfate inhalation solution may cause the following serious side effects:

• Worsening of the tightening and swelling of the muscles around your child's airways (bronchospasm).This side effect can be life threatening. Call your child's doctor or get emergency help right away if your child's breathing is not helped or gets worse during treatment with albuterol sulfate inhalation solution.
• Serious and life threatening allergic reactions. Symptoms of a serious allergic reaction include:
  • Hives, rash
  • Swelling of your child's face, eyelids, lips, tongue, or throat, and trouble swallowing
  • Worsening of your child's breathing problems such as wheezing, chest tightness or shortness of breath
  • Shock (loss of blood pressure and consciousness).

The most common side effects with albuterol sulfate inhalation solution include a fast or irregular heartbeat, chest pain, shakiness, or nervousness.

How should albuterol sulfate inhalation solution be stored?

• Store albuterol sulfate inhalation solution at room temperature, 2°C to 25°C (36°F to 77°F) in its tightly closed container.
• Protect vials from light before use. Therefore, keep unused vials in the foil pouch or carton. Once removed from the foil pouch, use vial(s) within one week.
• Do not use albuterol sulfate inhalation solution after the expiration (EXP) date printed on the vial. Do not use albuterol sulfate inhalation solution that is not clear and colorless.
• Safely, discard albuterol sulfate inhalation solution that is out-of-date or no longer needed.
• Keep albuterol sulfate inhalation solution and all medicines out of the reach of children.

General Information about albuterol sulfate inhalation solution

Medicines are sometimes prescribed for conditions that are not mentioned in the patient information leaflets. Do not use albuterol sulfate inhalation solution for a condition for which it was not prescribed. Do not give albuterol sulfate inhalation solution to other people, even if they have the same symptoms your child has. It may harm them.

This leaflet summarizes the most important information about albuterol sulfate inhalation solution. If you would like more information, talk with your child's doctor. You can ask your child's doctor or pharmacist for information about albuterol sulfate inhalation solution that is written for health professionals. You can also call the company that makes albuterol sulfate inhalation solution toll free at 1-866-850-2876.

What are the ingredients in albuterol sulfate inhalation solution?

Active Ingredient:albuterol sulfate

Inactive Ingredients:sodium chloride and sulfuric acid

Rx Only

Distributed by:

Aurobindo Pharma USA, Inc.

279 Princeton-Hightstown Road

East Windsor, NJ 08520



Manufactured by:

Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.

No.800, Haifa Road, Chengdu Cross-strait Science and Technology Industrial

Development Park, Wenjiang District, Chengdu, Sichuan

China 611130

Revised: July 2024

Read this patient information completely every time your prescription is filled as information may have changed. Keep these instructions with your medication, as you may want to read them again.

Albuterol sulfate inhalation solution should only be used under the direction of a physician. Your physician and pharmacist have more information about albuterol sulfate inhalation solution and the condition for which it has been prescribed. Contact them if you have additional questions.

Storing your Medicine

Store albuterol sulfate inhalation solution between 2°C and 25°C (36°F and 77°F). Vials should be protected from light before use, therefore, keep unused vials in the foil pouch. Do not use after the expiration (EXP) date printed on the vial.

Dose

Albuterol sulfate inhalation solution is supplied as a single-dose, ready-to-use vial containing 3 mL of solution. No mixing or dilution is needed. Use one new vial with each nebulizer treatment.

Instructions for Use

1. Remove one vial from the foil pouch. Place remaining vials back into foil pouch for storage.

2. Twist the cap completely off the vial and squeeze the contents into the nebulizer reservoir (Figure 1).

3. Connect the nebulizer to the mouthpiece or face mask (Figure 2).

4. Connect the nebulizer to the compressor.

5. Sit in a comfortable, upright position; place the mouthpiece in your mouth (Figure 3) or put on the face mask (Figure 4); and turn on the compressor.

6. Breathe as calmly, deeply and evenly as possible through your mouth until no more mist is formed in the nebulizer chamber (about 5 to 15 minutes). At this point, the treatment is finished.

7. Clean the nebulizer (see manufacturer's instructions).

Distributed by:

Aurobindo Pharma USA, Inc.

279 Princeton-Hightstown Road

East Windsor, NJ 08520



Manufactured by:

Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.

No.800, Haifa Road, Chengdu Cross-strait Science and Technology Industrial

Development Park, Wenjiang District, Chengdu, Sichuan

China 611130

Revised: July 2024

NDC 81894-105-05

Albuterol Sulfate

Inhalation Solution

0.63 mg*/3 mL

* Each unit dose vial contains 0.63 mg of

albuterolequivalent to 0.75 mg of albuterol sulfate.

For Inhalation only

Pouch contains: Five 3 mL vials

Rx only Sterile Unit-Dose Vials

AUROBINDO

NDC 81894-105-25

Albuterol Sulfate

Inhalation Solution

0.63 mg*/3 mL

* Each unit dose vial contains 0.63 mg of albuterol

equivalent to 0.75 mg of albuterol sulfate.

Sterile Unit-Dose Vials

For Inhalation only

ATTENTION PHARMACIST:

Detach the “Patient’s Instruction for Use” from

package insert and dispense with solution.

Carton contains: 5 pouches of Five 3 mL vials each

AUROBINDO

NDC 81894-105-30

Albuterol Sulfate

Inhalation Solution

0.63 mg*/3 mL

* Each unit dose vial contains 0.63 mg of albuterol

equivalent to 0.75 mg of albuterol sulfate.

Sterile Unit-Dose Vials

For Inhalation only

ATTENTION PHARMACIST:

Detach the “Patient’s Instruction for Use” from

package insert and dispense with solution.

Carton contains: 6 pouches of Five 3 mL vials each

AUROBINDO

NDC 81894-106-05

Albuterol Sulfate

Inhalation Solution

1.25 mg*/3 mL

* Each unit dose vial contains 1.25 mg of albuterol

equivalent to 1.5 mg of albuterol sulfate.

For Inhalation only

Pouch contains: Five 3 mL vials

Rx only Sterile Unit-Dose Vials

AUROBINDO

NDC 81894-106-25

Albuterol Sulfate

Inhalation Solution

1.25 mg*/3 mL

* Each unit dose vial contains 1.25 mg of albuterol

equivalent to 1.5 mg of albuterol sulfate.

Sterile Unit-Dose Vials

For Inhalation only

ATTENTION PHARMACIST:

Detach the “Patient’s Instruction for Use” from

package insert and dispense with solution.

Carton contains: 5 pouches of Five 3 mL vials each

AUROBINDO

NDC 81894-106-30

Albuterol Sulfate

Inhalation Solution

0.63 mg*/3 mL

* Each unit dose vial contains 0.63 mg of albuterol

equivalent to 0.75 mg of albuterol sulfate.

Sterile Unit-Dose Vials

For Inhalation only

ATTENTION PHARMACIST:

Detach the “Patient’s Instruction for Use” from

package insert and dispense with solution.

Carton contains: 6 pouches of Five 3 mL vials each

AUROBINDO