Heparin Sodium
- Product NDC
- 71872-7365
- 11-digit product format
- 718727365
- Labeler code
- 71872
- Product ID
- 71872-7365_4c118bb8-d002-3029-e063-6394a90a7d36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA202957
- Marketing category
- ANDA
- Marketing start
- 2014-06-12
- Substance
- HEPARIN SODIUM
- Active strength
- 1000 [USP'U]/mL
- Pharmacologic classes
- Anti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Heparin Sodium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HEPARIN SODIUM | 1000 [USP'U]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZZ45AB24CA |
| Rxcui | 1361226 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71872-7365-1 | Heparin Sodium | 10 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 10 | | 1 |
| 71872-7365-1 | Heparin Sodium | 1 in 1 BAG | INJECTION, SOLUTION | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7365-1 | 71872736501 | 1 VIAL, MULTI-DOSE in 1 BAG (71872-7365-1) / 10 mL in 1 VIAL, MULTI-DOSE | 2026-02-20 | No | No | Current |