Allopurinol
- Product NDC
- 50090-6968
- 11-digit product format
- 500906968
- Labeler code
- 50090
- Product ID
- 50090-6968_aaf62490-cdc7-4b5c-b665-2b901a8799f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204467
- Marketing category
- ANDA
- Marketing start
- 2022-07-01
- 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
openFDA Listing Details
- Product ID
- 50090-6968_aaf62490-cdc7-4b5c-b665-2b901a8799f2
- Product type
- HUMAN PRESCRIPTION DRUG
- Finished product
- Yes
- Brand name base
- Allopurinol
- Generic name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Marketing start
- 2022-07-01
- Marketing category
- ANDA
- Application number
- ANDA204467
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC]; Xanthine Oxidase Inhibitors [MoA]
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| ALLOPURINOL | 300 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 63CZ7GJN5I |
| Rxcui | 197320 |
| Spl Set Id | 420d338d-4d0d-4e38-bfe2-a83256821b45 |
| Manufacturer Name | A-S Medication Solutions |
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 |
|---|
| 50090-6968-0 | 50090696800 | 90 TABLET in 1 BOTTLE (50090-6968-0) | 90 tablet | 2023-12-21 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | A-S Medication Solutions | 2024-04-10 | Human Prescription Drug Label | 3 |