OMEPRAZOLE AND SODIUM BICARBONATE- omeprazole and sodium bicarbonate capsule 
Zydus Pharmaceuticals USA Inc.

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Omeprazole and Sodium Bicarbonate Capsules

Drug Facts

Active ingredients (in each capsule)

Omeprazole, USP ……………………………………….20 mg

Sodium Bicarbonate, USP …………………………....1100 mg

Purpose

Omeprazole, USP .............................................................................Acid reducer

Sodium Bicarbonate, USP ………Allows absorption of this omeprazole product

Use

Warnings

Allergy alert: Do not use if you are allergic to omeprazole

Do not use if you have:

These may be signs of a serious condition. See your doctor.

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are taking

a prescription drug. Acid reducers may interact with certain prescription drugs.

Stop use and ask a doctor if

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Directions

14 Day Course of Treatment

Repeated 14 Day Courses (if needed)

•  children under 18 years of age: ask a doctor.

   Heartburn in children may sometimes be caused by a serious condition.

Other information

Inactive ingredient

croscarmellose sodium, FD&C blue # 1, gelatin, magnesium stearate, polysorbate 80, sodium lauryl sulfate and titanium dioxide. The capsule shell is printed with black pharmaceutical ink which contains following ingredients: black iron oxide, butyl alcohol, dehydrated alcohol, isopropyl alcohol, potassium hydroxide, propylene glycol, purified water, shellac and strong ammonia solution.

Questions or comments?

Serious side effects associated with use of this drug product may be reported to this number: 1-877-993-8779 or visit www.zydususa.com

Hours of operation:

9:00 am to 5:00 pm

EST M-F.

You may report side effects to FDA at 1-800-FDA-1088.

How Omeprazole and Sodium Bicarbonate Capsule Works For Your Frequent Heartburn

Omeprazole and sodium bicarbonate capsule works differently from other OTC heartburn products, such as antacids and other acid reducers. Omeprazole and sodium bicarbonate capsule stops acid production at the source – the acid pump that produces stomach acid. Omeprazole and sodium bicarbonate capsule is to be used once a day (every 24 hours), every day for 14 days.

What to Expect When Using Omeprazole and Sodium Bicarbonate Capsule

Omeprazole and sodium bicarbonate capsule is a different type of medicine from antacids and other acid reducers. Omeprazole and sodium bicarbonate capsule may take 1 to 4 days for full effect, although some people get complete relief of symptoms within 24 hours. Make sure you take the entire 14 days of dosing to treat your frequent heartburn.

Tips for Managing Heartburn

How are Omeprazole and Sodium Bicarbonate Capsules Sold

Omeprazole and Sodium Bicarbonate Capsules, 20 mg/1100 mg are white to off-white fine powder filled in hard gelatin capsule shells of size '00' having an opaque white cap and an opaque white body printed with '503' on body in black ink and a blue tamper evident band and are available as follows:

NDC 68382-503-67 in one HDPE bottle of 14 capsules

NDC 68382-503-17 in two HDPE bottles of 28 capsules (one bottle contains 14 capsules)

NDC 68382-503-04 in three HDPE bottles of 42 capsules (one bottle contains 14 capsules)

Do not use for more than 14 days in a row unless directed by your doctor. For the 28 count (two 14 day courses) and the 42 count (three 14 day courses), you may repeat a 14 day course every 4 months.

Manufactured by:

Cadila Healthcare Ltd.

Ahmedabad, India

Distributed by:

Zydus Pharmaceuticals (USA) Inc.

Pennington, NJ 08534

Rev.: 02/19

Carton and container labels

NDC 68382-503-67

Omeprazole and Sodium Bicarbonate Capsules, 20 mg/1100 mg

14 Capsules

Zydus

Omeprazole and Sodium Bicarbonate Capsules, 20 mg/1100 mg
Omeprazole and Sodium Bicarbonate Capsules, 20 mg/1100 mg
OMEPRAZOLE AND SODIUM BICARBONATE 
omeprazole and sodium bicarbonate capsule
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68382-503
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OMEPRAZOLE (UNII: KG60484QX9) (OMEPRAZOLE - UNII:KG60484QX9) OMEPRAZOLE20 mg
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE1100 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GELATIN (UNII: 2G86QN327L)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
BUTYL ALCOHOL (UNII: 8PJ61P6TS3)  
ALCOHOL (UNII: 3K9958V90M)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SHELLAC (UNII: 46N107B71O)  
AMMONIA (UNII: 5138Q19F1X)  
Product Characteristics
ColorWHITE (OPAQUE WHITE) , WHITE (OPAQUE WHITE) Scoreno score
ShapeCAPSULE (CAPSULE) Size24mm
FlavorImprint Code 503
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68382-503-172 in 1 CARTON07/19/2018
114 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:68382-503-671 in 1 CARTON07/19/2018
214 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:68382-503-043 in 1 CARTON07/19/2018
314 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20334507/19/2018
Labeler - Zydus Pharmaceuticals USA Inc. (156861945)
Registrant - Zydus Worldwide DMCC (557951127)
Establishment
NameAddressID/FEIBusiness Operations
Zydus Lifesciences Limited918596198ANALYSIS(68382-503) , MANUFACTURE(68382-503)

Revised: 6/2023
Document Id: 07494f08-60c9-4350-a91e-944730e677e0
Set id: e90c63f2-33bf-4b61-beb2-70f592cd23a5
Version: 7
Effective Time: 20230606
 
Zydus Pharmaceuticals USA Inc.