Heparin Sodium
- Product NDC
- 52584-542
- 11-digit product format
- 525840542
- Labeler code
- 52584
- Product ID
- 52584-542_307bad1d-fb06-4a82-8d03-cdbb864e26c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- NDA017029
- Marketing category
- NDA
- Marketing start
- 2010-03-01
- Marketing end
- 2021-11-30
- Substance
- HEPARIN SODIUM
- Active strength
- 10000 [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 |
|---|
| 52584-542-01 | 52584054201 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-542-01) > 1 mL in 1 VIAL, MULTI-DOSE | 2015-04-01 | 2021-11-30 | No | No | Current |