Heparin Sodium
- Product NDC
- 71288-449
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Meitheal Pharmaceuticals Inc.
- Application
- ANDA211007
- Marketing category
- ANDA
- Substance
- HEPARIN SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71288-449-02 | 25 VIAL, MULTI-DOSE in 1 CARTON (71288-449-02) / 1 mL in 1 VIAL, MULTI-DOSE (71288-449-01) | 2025-07-02 | | 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 |