Heparin Sodium
- Product NDC
- 52584-402
- 11-digit product format
- 525840402
- Labeler code
- 52584
- Product ID
- 52584-402_c98d0321-df6c-44fd-8c4b-45d67c7393d7
- 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
- 2019-09-06
- Marketing end
- 2023-10-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-402-01 | 52584040201 | 1 VIAL in 1 BAG (52584-402-01) > 1 mL in 1 VIAL | 1 vial | 2019-09-06 | 0000-00-00 | No | No | Current |