Allopurinol
- Product NDC
- 50090-7351
- 11-digit product format
- 500907351
- Labeler code
- 50090
- Product ID
- 50090-7351_f3a7a6da-e2fe-4ad8-8c49-f5636b533f31
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA217748
- Marketing category
- ANDA
- Marketing start
- 2023-08-03
- Substance
- ALLOPURINOL
- Active strength
- 300 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 63CZ7GJN5I | ALLOPURINOL | 315-30-0 | ALLOPURINOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7351-0 | 50090735100 | 100 TABLET in 1 BOTTLE (50090-7351-0) | 100 tablet | 2024-10-16 | No | No | Historical |
| 50090-7351-1 | 50090735101 | 30 TABLET in 1 BOTTLE (50090-7351-1) | 30 tablet | 2024-10-16 | No | No | Historical |
| 50090-7351-3 | 50090735103 | 90 TABLET in 1 BOTTLE (50090-7351-3) | 90 tablet | 2024-10-16 | No | No | Historical |