Heparin Sodium
- Product NDC
- 67457-953
- 11-digit product format
- 674570953
- Labeler code
- 67457
- Product ID
- 67457-953_c1c9c265-453e-4464-8b8f-682b3fb42f0a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA203851
- Marketing category
- ANDA
- Marketing start
- 2019-04-30
- Marketing end
- 2021-09-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67457-953-10 | 67457095310 | 25 VIAL, MULTI-DOSE in 1 CARTON (67457-953-10) > 10 mL in 1 VIAL, MULTI-DOSE (67457-953-00) | 2019-04-30 | 2021-09-30 | No | No | Current |