Warfarin Sodium
- Product NDC
- 63629-6342
- 11-digit product format
- 636296342
- Labeler code
- 63629
- Product ID
- 63629-6342_08e46109-a1b4-429e-a4e8-d01606144e17
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202202
- Marketing category
- ANDA
- Marketing start
- 2010-08-16
- Marketing end
- 0000-00-00
- Substance
- WARFARIN SODIUM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-6342-1 | 63629634201 | 60 TABLET in 1 BOTTLE (63629-6342-1) | 60 tablet | 2017-02-14 | 0000-00-00 | No | No | Current |
| 63629-6342-2 | 63629634202 | 90 TABLET in 1 BOTTLE (63629-6342-2) | 90 tablet | 2015-09-17 | 0000-00-00 | No | No | Current |