![HEPARIN SODIUM INJECTION, SOLUTION [CANTRELL DRUG COMPANY]](https://medic.hrt.org//dailymed/images/fda3f337-deab-40f3-bc0d-0c08baeb8a2d/52533-216-40.jpg)
| NDC | 52533-216-40 |
| Set ID | fda3f337-deab-40f3-bc0d-0c08baeb8a2d |
| 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:52533-216 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin 50 [USP'U] in 1 mL Inactive Ingredients Ingredient Name Strength Sodium Chloride (UNII: 451W47IQ8X) 4.5 mg in 1 mL BENZYL ALCOHOL (UNII: LKG8494WBH) 0.0001 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:52533-216-40 500 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2012 Labeler - Cantrell Drug Company (035545763)
