NDC | 52533-098-30 |
Set ID | 69333d0f-8bee-4975-9d3c-0fa7027ddfea |
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:52533-098 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin 10 [USP'U] in 1 mL Inactive Ingredients Ingredient Name Strength Sodium Chloride (UNII: 451W47IQ8X) 9 mg in 1 mL BENZYL ALCOHOL (UNII: LKG8494WBH) 0.001 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:52533-098-30 500 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/30/2011 Labeler - Cantrell Drug Company (035545763) Establishment Name Address ID/FEI Business Operations Cantrell Drug Company 035545763 manufacture(52533-098) , human drug compounding outsourcing facility(52533-098) (No intent to compound 506E (drug shortage) drugs), (Not compounding from bulk ingredient)