Allopurinol
- Product NDC
- 68788-6422
- 11-digit product format
- 687886422
- Labeler code
- 68788
- Product ID
- 68788-6422_9aa81042-818a-41bf-a05f-1d8d177e7d09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA018659
- Marketing category
- ANDA
- Marketing start
- 2016-06-14
- Marketing end
- 0000-00-00
- Substance
- ALLOPURINOL
- Active strength
- 300 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record