Allopurinol
- Product NDC
- 70518-1407
- 11-digit product format
- 705181407
- Labeler code
- 70518
- Product ID
- 70518-1407_92bcb0d9-1374-579a-e053-2a95a90abe2d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA018659
- Marketing category
- ANDA
- Marketing start
- 2018-09-10
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record