Warfarin Sodium
- Product NDC
- 68071-4385
- 11-digit product format
- 680714385
- Labeler code
- 68071
- Product ID
- 68071-4385_d5cbbf1b-6fdb-f7cd-e053-2995a90a5e33
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090935
- Marketing category
- ANDA
- Marketing start
- 2011-11-01
- Marketing end
- 0000-00-00
- Substance
- WARFARIN SODIUM
- Active strength
- 3 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
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 |
|---|
| 68071-4385-3 | 68071438503 | 30 TABLET in 1 BOTTLE (68071-4385-3) | 30 tablet | 2018-04-10 | 0000-00-00 | No | No | Current |
| 68071-4385-9 | 68071438509 | 90 TABLET in 1 BOTTLE (68071-4385-9) | 90 tablet | 2018-04-10 | 0000-00-00 | No | No | Current |