Febuxostat
- Product NDC
- 63304-864
- 11-digit product format
- 633040864
- Labeler code
- 63304
- Product ID
- 63304-864_d618acad-1835-4148-a345-aa1054c367ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Febuxostat
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Ranbaxy Pharmaceuticals Inc.
- Application
- ANDA205392
- Marketing category
- ANDA
- Marketing start
- 2015-01-17
- Marketing end
- 0000-00-00
- Substance
- FEBUXOSTAT
- Active strength
- 40 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#