Heparin Sodium
- Product NDC
- 48433-329
- 11-digit product format
- 484330329
- Labeler code
- 48433
- Product ID
- 48433-329_804e4e29-aadc-4eed-8210-b7013a4a384e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Safecor Health, LLC
- Application
- ANDA202957
- Marketing category
- ANDA
- Marketing start
- 2014-09-30
- Marketing end
- 0000-00-00
- Substance
- HEPARIN SODIUM
- Active strength
- 5000 [USP'U]/mL
- Pharmacologic classes
- Anti-coagulant [EPC],Heparin [CS],Unfractionated Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record