NDC | 52533-211-26 |
Set ID | dbe6b79b-9eed-47d5-9a0a-8ca345d77634 |
Category | HUMAN PRESCRIPTION DRUG LABEL |
Packager | Cantrell Drug Company |
Generic Name | |
Product Class | Anti-coagulant |
Product Number | |
Application Number |
- PRINCIPAL DISPLAY PANEL
- SPL UNCLASSIFIED SECTION
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INGREDIENTS AND APPEARANCE
HEPARIN SODIUM
heparin sodium injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-211 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin 4 [USP'U] in 1 mL Inactive Ingredients Ingredient Name Strength Sodium Chloride (UNII: 451W47IQ8X) 4.5 mg in 1 mL BENZYL ALCOHOL (UNII: LKG8494WBH) 0.00004 mL in 1 mL Water (UNII: 059QF0KO0R) Other Ingredients Ingredient Kind Ingredient Name Quantity May contain HYDROCHLORIC ACID (UNII: QTT17582CB) May contain SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52533-211-26 1000 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/13/2012 Labeler - Cantrell Drug Company (035545763)