![HEPARIN SODIUM INJECTION, SOLUTION [CANTRELL DRUG COMPANY]](https://medic.hrt.org//dailymed/images/50f57038-6652-47e1-a834-d524b9a86b31/52533-148-16.jpg)
| NDC | 52533-148-16 |
| Set ID | 50f57038-6652-47e1-a834-d524b9a86b31 |
| Category | HUMAN PRESCRIPTION DRUG LABEL |
| Packager | Cantrell Drug Company |
| Generic Name | |
| Product Class | Anti-coagulant |
| Product Number | |
| Application Number |
- Label
- SPL UNCLASSIFIED SECTION
-
INGREDIENTS AND APPEARANCE
HEPARIN SODIUM
heparin sodium injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-148 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Heparin Sodium (UNII: ZZ45AB24CA) (Heparin - UNII:T2410KM04A) Heparin 0.5 [USP'U] in 1 mL Inactive Ingredients Ingredient Name Strength Sodium Chloride (UNII: 451W47IQ8X) 4.5 mg 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:52533-148-16 2 mL in 1 SYRINGE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/22/2012 Labeler - Cantrell Drug Company (035545763)
