Enoxaparin Sodium
- Product NDC
- 0703-8680
- 11-digit product format
- 007038680
- Labeler code
- 0703
- Product ID
- 0703-8680_56b5e192-d56a-4f4b-9400-5cb50c6feac8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enoxaparin Sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Teva Parenteral Medicines, Inc.
- Application
- ANDA076726
- Marketing category
- ANDA
- Marketing start
- 2014-12-19
- Marketing end
- 2022-09-30
- Substance
- ENOXAPARIN SODIUM
- Active strength
- 80 mg/.8mL
- 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 |
|---|
| 0703-8680-23 | 00703868023 | 10 SYRINGE in 1 CARTON (0703-8680-23) > .8 mL in 1 SYRINGE (0703-8680-21) | 10 syringe | 2014-12-19 | 0000-00-00 | No | No | Current |