FEBUXOSTAT
- Product NDC
- 48792-7906
- 11-digit product format
- 487927906
- Labeler code
- 48792
- Product ID
- 48792-7906_a78dd053-c69a-15ba-e053-2a95a90aadb9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- febuxostat
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sunshine Lake Pharma Co., Ltd.
- Application
- ANDA213069
- Marketing category
- ANDA
- Marketing start
- 2020-06-02
- Marketing end
- 0000-00-00
- Substance
- FEBUXOSTAT
- Active strength
- 80 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 48792-7906-1 | 48792790601 | 30 TABLET in 1 BOTTLE (48792-7906-1) | 30 tablet | 2020-06-02 | 0000-00-00 | No | No | Current |