Heparin Sodium
- Product NDC
- 55154-9354
- 11-digit product format
- 551549354
- Labeler code
- 55154
- Product ID
- 55154-9354_640ea044-c7c9-40df-85a3-585c71f5360c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HEPARIN SODIUM
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Cardinal Health
- Application
- NDA017029
- Marketing category
- NDA
- Marketing start
- 2010-06-18
- Marketing end
- 2021-08-31
- 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 |
|---|
| 55154-9354-5 | 55154935405 | 5 VIAL in 1 BAG (55154-9354-5) > 1 mL in 1 VIAL | 5 vial | 2010-06-18 | 2021-08-31 | No | No | Current |