Enoxaparin Sodium
- Product NDC
- 60505-0791
- 11-digit product format
- 605050791
- Labeler code
- 60505
- Product ID
- 60505-0791_86fde550-ac79-87d9-be58-6d10e4b74e77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- enoxaparin sodium
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- Apotex Corp.
- Application
- ANDA078990
- Marketing category
- ANDA
- Marketing start
- 2019-01-31
- Marketing end
- 0000-00-00
- Substance
- ENOXAPARIN SODIUM
- Active strength
- 30 mg/.3mL
- Pharmacologic classes
- Heparin, Low-Molecular-Weight [CS], Low Molecular Weight Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-0791-0 | 60505079100 | 1 SYRINGE in 1 CARTON (60505-0791-0) > .3 mL in 1 SYRINGE | 1 syringe | 2019-01-31 | 0000-00-00 | No | No | Current |
| 60505-0791-4 | 60505079104 | 10 SYRINGE in 1 CARTON (60505-0791-4) > .3 mL in 1 SYRINGE | 10 syringe | 2019-01-31 | 0000-00-00 | No | No | Current |