Warfarin Sodium
- Product NDC
- 50090-5439
- 11-digit product format
- 500905439
- Labeler code
- 50090
- Product ID
- 50090-5439_0ab1fd84-65f5-471a-8482-639e657aa1cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040616
- Marketing category
- ANDA
- Marketing start
- 2015-04-07
- Marketing end
- 0000-00-00
- Substance
- WARFARIN SODIUM
- Active strength
- 5 mg/1
- Pharmacologic classes
- Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5439-0 | 50090543900 | 30 TABLET in 1 BOTTLE (50090-5439-0) | 30 tablet | 2021-01-20 | 0000-00-00 | No | No | Current |
| 50090-5439-1 | 50090543901 | 60 TABLET in 1 BOTTLE (50090-5439-1) | 60 tablet | 2019-05-31 | 0000-00-00 | No | No | Current |
| 50090-5439-2 | 50090543902 | 90 TABLET in 1 BOTTLE (50090-5439-2) | 90 tablet | 2021-01-20 | 0000-00-00 | No | No | Current |