Warfarin Sodium
- Product NDC
- 50090-3110
- 11-digit product format
- 500903110
- Labeler code
- 50090
- Product ID
- 50090-3110_f3871ac8-cab5-4db4-9e5d-24f76da67ff2
- 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
- 2015-10-19
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50090-3110-0 | 50090311000 | 30 TABLET in 1 BOTTLE (50090-3110-0) | 30 tablet | 2019-10-09 | 0000-00-00 | No | No | Current |
| 50090-3110-1 | 50090311001 | 100 TABLET in 1 BOTTLE (50090-3110-1) | 100 tablet | 2017-07-31 | 0000-00-00 | No | No | Current |