Heparin Sodium
- Product NDC
- 71288-451
- 11-digit product format
- 712880451
- Labeler code
- 71288
- Product ID
- 71288-451_505f018d-608d-4dd4-b7b9-640b25b0fc44
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Meitheal Pharmaceuticals Inc.
- Application
- ANDA211007
- Marketing category
- ANDA
- Marketing start
- 2025-07-02
- Substance
- HEPARIN SODIUM
- Active strength
- 10000 [USP'U]/mL
- Pharmacologic classes
- Anti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 |
|---|
| 71288-451-02 | 71288045102 | 25 VIAL, MULTI-DOSE in 1 CARTON (71288-451-02) / 1 mL in 1 VIAL, MULTI-DOSE (71288-451-01) | 2025-07-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Heparin Sodium | Meitheal Pharmaceuticals Inc. | Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd. | 2025-09-26 | HUMAN PRESCRIPTION DRUG LABEL | 12 |