Heparin Sodium
- Product NDC
- 52584-111
- 11-digit product format
- 525840111
- Labeler code
- 52584
- Product ID
- 52584-111_7cb0f29a-4394-441f-b4f9-ec444b1f1f70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- heparin sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- NDA017029
- Marketing category
- NDA
- Marketing start
- 2021-08-26
- Marketing end
- 2023-08-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-111-03 | 52584011103 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-111-03) > 1 mL in 1 VIAL, MULTI-DOSE | 2021-08-26 | 0000-00-00 | No | No | Current |