HEPARIN SODIUM
- Product NDC
- 52584-116
- 11-digit product format
- 525840116
- Labeler code
- 52584
- Product ID
- 52584-116_618038b0-0f70-485d-99e1-6d33604c7c51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- heparin sodium injection
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA203851
- Marketing category
- ANDA
- Marketing start
- 2021-02-23
- Marketing end
- 2023-11-30
- 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 |
|---|
| 52584-116-02 | 52584011602 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-116-02) > 1 mL in 1 VIAL, SINGLE-DOSE | 2021-02-23 | 2023-11-30 | No | No | Current |