Heparin Sodium
- Product NDC
- 70518-4547
- 11-digit product format
- 705184547
- Labeler code
- 70518
- Product ID
- 70518-4547_4885975b-67c0-5519-e063-6394a90a105b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- REMEDYREPACK INC.
- Application
- NDA017037
- Marketing category
- NDA
- Marketing start
- 2026-01-16
- Substance
- HEPARIN SODIUM
- Active strength
- 5000 [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 | 5000 [USP'U]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZZ45AB24CA |
| Rxcui | 1659263 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4547-0 | Heparin Sodium | 25 in 1 PACKAGE | INJECTION | 25 | | 1 |
| 70518-4547-1 | Heparin Sodium | 1 mL in 1 VIAL | INJECTION | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4547-0 | 70518454700 | 25 VIAL in 1 PACKAGE (70518-4547-0) / 1 mL in 1 VIAL (70518-4547-1) | 25 vial | 2026-01-16 | No | No | Current |
| 70518-4547-1 | 70518454701 | 1 mL in 1 VIAL | 1 ml | | | | Historical |