Label: CYANOCOBALAMIN injection, solution

  • NDC Code(s): 63323-044-41, 63323-044-44
  • Packager: Fresenius Kabi USA, LLC
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated September 3, 2018

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    Cyanocobalamin Injection, USP is a sterile solution of cyanocobalamin for intramuscular or subcutaneous use.

    Each mL contains 1000 mcg cyanocobalamin; sodium chloride 0.9%; benzyl alcohol 1.5%; Water for Injection q.s.  Hydrochloric acid and/or sodium hydroxide for pH adjustment if necessary (4.5-7.0).

    Cyanocobalamin appears as dark, red crystals or as an amorphous or crystalline, red powder.  It is very hygroscopic in the anhydrous form, and sparingly soluble in water (1:80).  It is stable to autoclaving for short periods at 121°C.  The Vitamin B12 coenzymes are very unstable in light.

    The chemical name is 5,6-dimethyl-benzimidazolyl cyanocobamide.  The cobalt content is 4.34%.  The structural formula is represented below:



    Vitamin B12 is essential to growth, cell reproduction, hematopoiesis, nucleoprotein and myelin synthesis.

    Cyanocobalamin is quantitatively and rapidly absorbed from intramuscular and subcutaneous sites of injection; the plasma level of the compound reaches its peak within one hour after intramuscular injection. Absorbed Vitamin B12 is transported via specific B12 binding proteins, transcobalamin I and II to the various tissues.  The liver is the main organ for Vitamin B12 storage.

    Within 48 hours after injection of 100 or 1000 mcg of Vitamin B12, 50 to 98% of the injected dose may appear in the urine.  The major portion is excreted within the first eight hours. Intravenous administration results in even more rapid excretion with little opportunity for liver storage.

    Gastrointestinal absorption of Vitamin B12 depends on the presence of sufficient intrinsic factor and calcium ions.  Intrinsic factor deficiency causes pernicious anemia, which may be associated with subacute combined degeneration of the spinal cord.  Prompt parenteral administration of Vitamin B12 prevents progression of neurologic damage.

    The average diet supplies about 5 to 15 mcg/day of Vitamin B12 in a protein-bound form that is available for absorption after normal digestion.  Vitamin B12 is not present in foods of plant origin, but is abundant in foods of animal origin.  In people with normal absorption, deficiencies have been reported only in strict vegetarians who consume no products of animal origin (including no milk products or eggs).

    Vitamin B12 is bound to intrinsic factor during transit through the stomach; separation occurs in the terminal ileum in the presence of calcium, and Vitamin B12 enters the mucosal cell for absorption.  It is then transported by the transcobalamin binding proteins.  A small amount (approximately 1% of the total amount ingested) is absorbed by simple diffusion, but this mechanism is adequate only with very large doses.  Oral absorption is considered too undependable to rely on in patients with pernicious anemia or other conditions resulting in malabsorption of Vitamin B12.

    Cyanocobalamin is the most widely used form of Vitamin B12, and has hematopoietic activity apparently identical to that of the antianemia factor in purified liver extract.  Hydroxocobalamin is equally as effective as cyanocobalamin, and they share the cobalamin molecular structure.


    Cyanocobalamin is indicated for Vitamin B12 deficiencies due to malabsorption which may be associated with the following conditions:

                Addisonian (pernicious) anemia

                Gastrointestinal pathology, dysfunction, or surgery, including gluten enteropathy or sprue, small bowel bacterial overgrowth, total or partial gastrectomy

                Fish tapeworm infestation

                Malignancy of pancreas or bowel

                Folic acid deficiency

    It may be possible to treat the underlying disease by surgical correction of anatomic lesions leading to small bowel bacterial overgrowth, expulsion of fish tapeworm, discontinuation of drugs leading to vitamin malabsorption (see Drug/Laboratory Test Interactions), use of a gluten-free diet in nontropical sprue, or administration of antibiotics in tropical sprue.  Such measures remove the need for long-term administration of cyanocobalamin.

    Requirements of Vitamin B12 in excess of normal (due to pregnancy, thyrotoxicosis, hemolytic anemia, hemorrhage, malignancy, hepatic and renal disease) can usually be met with oral supplementation.

    Cyanocobalamin injection is also suitable for the Vitamin B12 absorption test (Schilling test).


    Sensitivity to cobalt and/or Vitamin B12 is a contraindication.


    WARNING: This product contains aluminum that may be toxic.  Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired.  Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum.

    Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity.  Tissue loading may occur at even lower rates of administration.

    Patients with early Leber’s disease (hereditary optic nerve atrophy) who were treated with cyanocobalamin suffered severe and swift optic atrophy.

    Hypokalemia and sudden death may occur in severe megaloblastic anemia which is treated intensely.

    Anaphylactic shock and death have been reported after parenteral Vitamin B12 administration.  An intradermal test dose is recommended before cyanocobalamin injection is administered to patients suspected of being sensitive to this drug.

    This product contains benzyl alcohol.  Benzyl alcohol has been reported to be associated with a fatal ‘‘Gasping Syndrome’’ in premature infants.



    Vitamin B12 deficiency that is allowed to progress for longer than three months may produce permanent degenerative lesions of the spinal cord.  Doses of folic acid greater than 0.1 mg/day may result in hematologic remission in patients with Vitamin B12 deficiency.  Neurologic manifestations will not be prevented with folic acid, and if not treated with Vitamin B12, irreversible damage will result.

    Doses of cyanocobalamin exceeding 10 mcg daily may produce hematologic response in patients with folate deficiency.  Indiscriminate administration may mask the true diagnosis.

    Information for Patients

    Patients with pernicious anemia should be instructed that they will require monthly injections of Vitamin B12 for the remainder of their lives.  Failure to do so will result in return of the anemia and in development of incapacitating and irreversible damage to the nerves of the spinal cord.  Also, patients should be warned about the danger of taking folic acid in place of Vitamin B12, because the former may prevent anemia but allow progression of subacute combined degeneration.

    A vegetarian diet which contains no animal products (including milk products or eggs) does not supply any Vitamin B12.  Patients following such a diet should be advised to take oral Vitamin B12 regularly.  The need for Vitamin B12 is increased by pregnancy and lactation.  Deficiency has been recognized in infants of vegetarian mothers who were breast fed, even though the mothers had no symptoms of deficiency at the time.

    Laboratory Tests

    During the initial treatment of patients with pernicious anemia, serum potassium must be observed closely the first 48 hours and potassium replaced if necessary.

    Hematocrit, reticulocyte count, Vitamin B12, folate and iron levels should be obtained prior to treatment.  Hematocrit and reticulocyte counts should be repeated daily from the 5th to 7th days of therapy and then frequently until the hematocrit is normal.  If folate levels are low, folic acid should also be administered.  If reticulocytes have not increased after treatment or if reticulocyte counts do not continue at least twice normal as long as the hematocrit is less than 35%, diagnosis or treatment should be reevaluated.  Repeat determinations of iron and folic acid may reveal a complicating illness that might inhibit the response of the marrow.

    Patients with pernicious anemia have about three times the incidence of carcinoma of the stomach as the general population, so appropriate tests for this condition should be carried out when indicated.

    Drug/Laboratory Test Interactions

    Persons taking most antibiotics, methotrexate and pyrimethamine invalidate folic acid and Vitamin B12 diagnostic blood assays.

    Colchicine, para-aminosalicylic acid and heavy alcohol intake for longer than two weeks may produce malabsorption of Vitamin B12.

    Carcinogenesis, Mutagenesis

    Long-term studies in animals to evaluate carcinogenic potential have not been done.  There is no evidence from long-term use in patients with pernicious anemia that cyanocobalamin is carcinogenic.  Pernicious anemia is associated with an increased incidence of carcinoma of the stomach, but this is believed to be related to the underlying pathology and not to treatment with cyanocobalamin.


    Pregnancy Category C—Adequate and well-controlled studies have not been done in pregnant women.  However, Vitamin B12 is an essential vitamin and requirements are increased during pregnancy.  Amounts of Vitamin B12 that are recommended by the Food and Nutrition Board, National Academy of Science-National Research Council for pregnant women (4 mcg daily) should be consumed during pregnancy.

    Nursing Mothers

    Vitamin B12 is known to be excreted in human milk.  Amounts of Vitamin B12 that are recommended by the Food and Nutrition Board, National Academy of Science-National Research Council for lactating women (4 mcg daily) should be consumed during lactation.

    Pediatric Use

    Intake in children should be in the amount (0.5 to 3 mcg daily) recommended by the Food and Nutrition Board, National Academy of Science-National Research Council.



    Anaphylactic shock and death have been reported with administration of parenteral Vitamin B12 (see WARNINGS).


    Pulmonary edema and congestive heart failure early in treatment; peripheral vascular thrombosis.


    Polycythemia vera.


    Mild transient diarrhea.


    Itching; transitory exanthema.


    Feeling of swelling of entire body.


    No overdosage has been reported with this drug.


    Avoid using the intravenous route.  Use of this product intravenously will result in almost all of the vitamin being lost in the urine.

    Pernicious Anemia

    Parenteral Vitamin B12 is the recommended treatment and will be required for the remainder of the patient’s life.  The oral form is not dependable.  A dose of 100 mcg daily for six or seven days should be administered by intramuscular or deep subcutaneous injection.  If there is clinical improvement and if a reticulocyte response is observed, the same amount may be given on alternate days for seven doses, then every three to four days for another two to three weeks.  By this time hematologic values should have become normal.  This regimen should be followed by 100 mcg monthly for life.  Folic acid should be administered concomitantly if needed.

    Patients With Normal Intestinal Absorption

    Where the oral route is not deemed adequate, initial treatment similar to that for patients with pernicious anemia may be indicated depending on the severity of the deficiency.  Chronic treatment should be with an oral B12 preparation.  If other vitamin deficiencies are present, they should be treated.

    Schilling test

    The flushing dose is 1000 mcg.

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.


     Cyanocobalamin Injection, USP is supplied as follows:

    Product Code
    Unit of Sale
    Unit of 25
    1,000 mcg per mL
    1 mL fill in a 2 mL vial
    1 mL Multiple Dose Vial

    Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
    Use only if solution is clear and seal intact.
    PREMIERProRx® is a registered trademark of Premier Healthcare Alliance, L.P., used under license.


    Manufactured by:
    Fresenius Kabi
    Lake Zurich, IL 60047


    Issued: August 2018



    PACKAGE LABEL - PRINCIPAL DISPLAY - Cyanocobalamin 1 mL Multiple Dose Vial Label

    NDC 63323-044-41



    1,000 mcg/mL

    For IM or SC Use

    1 mL Multiple Dose Vial


    Rx only


    PACKAGE LABEL - PRINCIPAL DISPLAY - Cyanocobalamin 1 mL Multiple Dose Vial Tray Label

    NDC 63323-044-44


    1, 000 mcg/mL

    For IM or SC Use

    25 x 1 mL Multiple Dose Vials

    Rx only


    cyanocobalamin injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:63323-044
    Route of AdministrationINTRAMUSCULAR, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 9 mg  in 1 mL
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63323-044-4425 in 1 TRAY10/18/2000
    1NDC:63323-044-411 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Labeler - Fresenius Kabi USA, LLC (608775388)
    NameAddressID/FEIBusiness Operations
    Fresenius Kabi USA, LLC840771732MANUFACTURE(63323-044)