Heparin Sodium
- Product NDC
- 65219-066
- 11-digit product format
- 652190066
- Labeler code
- 65219
- Product ID
- 65219-066_f9aafe50-c679-4991-93ab-1866d5b19c8e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HEPARIN SODIUM
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Fresenius Kabi USA, LLC
- Application
- NDA017029
- Marketing category
- NDA
- Marketing start
- 2022-03-22
- 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
- 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 |
|---|
| 65219-066-10 | 65219006610 | 25 VIAL in 1 TRAY (65219-066-10) / 1 mL in 1 VIAL (65219-066-01) | 25 vial | 2022-03-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Heparin Sodium | Fresenius Kabi USA, LLC | 2024-01-05 | HUMAN PRESCRIPTION DRUG LABEL | 2 |