HEPARIN SODIUM
- Product NDC
- 52584-400
- 11-digit product format
- 525840400
- Labeler code
- 52584
- Product ID
- 52584-400_674b6a57-5ce7-4639-a970-bf433cb8e295
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- heparin sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA090808
- Marketing category
- ANDA
- Marketing start
- 2011-09-13
- Marketing end
- 2022-10-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-400-01 | 52584040001 | 1 VIAL in 1 BAG (52584-400-01) > 1 mL in 1 VIAL | 1 vial | 2011-09-13 | 2022-10-31 | No | No | Current |