Heparin Sodium
- Product NDC
- 55154-2380
- 11-digit product format
- 551542380
- Labeler code
- 55154
- Product ID
- 55154-2380_a37c938e-cc5d-4f8b-aa76-f1fc110d8e1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA089522
- Marketing category
- ANDA
- Marketing start
- 2009-12-07
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55154-2380-5 | 55154238005 | 5 CARTRIDGE in 1 BAG (55154-2380-5) / .5 mL in 1 CARTRIDGE | 5 cartridge | 2009-12-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Heparin Sodium | Cardinal Health 107, LLC | 2025-08-22 | HUMAN PRESCRIPTION DRUG LABEL | 16 |
| Heparin Sodium | Cardinal Health 107, LLC | 2024-09-05 | HUMAN PRESCRIPTION DRUG LABEL | 15 |