Heparin Sodium and Sodium Chloride
- Product NDC
- 0338-9552
- 11-digit product format
- 003389552
- Labeler code
- 0338
- Product ID
- 0338-9552_4c7da5eb-fae8-4b18-9a17-6e4a3a193c8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- heparin sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
- Marketing start
- 2017-10-25
- Marketing end
- 0000-00-00
- Substance
- HEPARIN SODIUM
- Active strength
- 2000 [iU]/1000mL
- Pharmacologic classes
- Anti-coagulant [EPC],Heparin [CS],Unfractionated Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record