Heparin Sodium
- Product NDC
- 55154-6996
- 11-digit product format
- 551546996
- Labeler code
- 55154
- Product ID
- 55154-6996_5cb136e6-833f-404a-8a3e-9645f1d18c4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Cardinal Health
- Application
- ANDA088100
- Marketing category
- ANDA
- Marketing start
- 2005-01-31
- Marketing end
- 2021-02-28
- 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 |
|---|
| 55154-6996-5 | 55154699605 | 5 CARTRIDGE in 1 BAG (55154-6996-5) > 1 mL in 1 CARTRIDGE | 5 cartridge | 2005-01-31 | 2021-02-28 | No | No | Current |