Heparin Sodium
- Product NDC
- 0641-6204
- 11-digit product format
- 006416204
- Labeler code
- 0641
- Product ID
- 0641-6204_3d3993a7-2f8d-4124-9065-1759b0d98aaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- NDA017037
- Marketing category
- NDA
- Marketing start
- 2020-01-14
- Substance
- HEPARIN SODIUM
- Active strength
- 5000 [USP'U]/.5mL
- Pharmacologic classes
- Anti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| ZZ45AB24CA | HEPARIN SODIUM | 9041-08-1 | HEPARIN SODIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0641-6204-10 | 00641620410 | 10 SYRINGE, GLASS in 1 CARTON (0641-6204-10) / .5 mL in 1 SYRINGE, GLASS (0641-6204-01) | 2020-01-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Heparin Sodium | Hikma Pharmaceuticals USA Inc. | 2025-08-13 | HUMAN PRESCRIPTION DRUG LABEL | 17 |