Heparin Sodium
- Product NDC
- 0781-3327
- 11-digit product format
- 007813327
- Labeler code
- 0781
- Product ID
- 0781-3327_acd26ba3-bd84-48db-9824-07984dfb11df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Sandoz Inc
- Application
- ANDA091682
- Marketing category
- ANDA
- Marketing start
- 2011-06-08
- Marketing end
- 2020-04-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record