Heparin Sodium
- Product NDC
- 66298-5197
- 11-digit product format
- 662985197
- Labeler code
- 66298
- Product ID
- 66298-5197_e838898f-646a-466f-8ffa-7ee3f5023d5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Fresenius Kabi Norge AS
- Application
- ANDA212441
- Marketing category
- ANDA
- Marketing start
- 2020-07-24
- Marketing end
- 0000-00-00
- Substance
- HEPARIN SODIUM
- Active strength
- 200 [USP'U]/100mL
- Pharmacologic classes
- Anti-coagulant [EPC],Heparin [CS],Unfractionated Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 66298-5197-7 | 66298519707 | 24 BAG in 1 CASE (66298-5197-7) > 500 mL in 1 BAG | 24 bag | 2020-07-24 | 0000-00-00 | No | No | Current |