Enoxaparin Sodium
- Product NDC
- 0781-3612
- 11-digit product format
- 007813612
- Labeler code
- 0781
- Product ID
- 0781-3612_d1e796d4-7266-4a8a-9327-7afb99ad80bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enoxaparin Sodium
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- Sandoz Inc
- Application
- ANDA077857
- Marketing category
- ANDA
- Marketing start
- 2010-07-23
- Marketing end
- 2023-05-31
- Substance
- ENOXAPARIN SODIUM
- Active strength
- 150 mg/mL
- Pharmacologic classes
- Heparin, Low-Molecular-Weight [CS],Low Molecular Weight Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0781-3612-68 | 00781361268 | 10 SYRINGE in 1 CARTON (0781-3612-68) > .8 mL in 1 SYRINGE (0781-3612-04) | 10 syringe | 2010-07-23 | 2023-05-31 | No | No | Current |