Heparin Sodium
- Product NDC
- 0409-1005
- 11-digit product format
- 004091005
- Labeler code
- 0409
- Product ID
- 0409-1005_ecaae7d2-a76e-4eca-b045-6c88d7c2ab8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HEPARIN SODIUM
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- NDA018916
- Marketing category
- NDA
- Marketing start
- 2023-02-27
- Substance
- HEPARIN SODIUM
- Active strength
- 200 [USP'U]/100mL
- Pharmacologic classes
- Anti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 0409-1005-20 | 00409100520 | 20 POUCH in 1 CASE (0409-1005-20) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-1005-01) | 20 pouch | 2023-02-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Heparin Sodium | Hospira, Inc. | 2026-05-12 | HUMAN PRESCRIPTION DRUG LABEL | 34 |