Allopurinol
- Product NDC
- 71921-241
- 11-digit product format
- 719210241
- Labeler code
- 71921
- Product ID
- 71921-241_88cf17e7-9773-490a-992b-63525120cadc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Florida Pharmaceutical Products, LLC
- Application
- ANDA204467
- Marketing category
- ANDA
- Marketing start
- 2025-05-22
- Substance
- ALLOPURINOL
- Active strength
- 200 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Allopurinol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLOPURINOL | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 63CZ7GJN5I |
| Rxcui | 197319, 197320, 245422 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71921-241-09 | Allopurinol | 90 in 1 BOTTLE | TABLET | 90 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71921-241-09 | 71921024109 | 90 TABLET in 1 BOTTLE (71921-241-09) | 90 tablet | 2025-05-22 | No | No | Historical |