ALLOPURINOL
- Product NDC
- 72189-417
- 11-digit product format
- 721890417
- Labeler code
- 72189
- Product ID
- 72189-417_4c4bb472-bcf4-c5df-e063-6394a90a787d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALLOPURINOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA204467
- Marketing category
- ANDA
- Marketing start
- 2023-02-02
- Marketing end
- 2029-10-31
- Substance
- ALLOPURINOL
- Active strength
- 300 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ALLOPURINOL
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLOPURINOL | 300 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 63CZ7GJN5I |
| Rxcui | 197320 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-417-30 | ALLOPURINOL | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 72189-417-90 | ALLOPURINOL | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-417 | ALLOPURINOL TABLET [DIRECT_RX] | 2 | Current NDC, 2 package rows | 20250123_f3bd5852-8e43-6b5d-e053-2995a90a194f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-417-30 | 72189041730 | 30 TABLET in 1 BOTTLE (72189-417-30) | 30 tablet | 2023-02-02 | 2029-10-31 | No | No | Historical |
| 72189-417-90 | 72189041790 | 90 TABLET in 1 BOTTLE (72189-417-90) | 90 tablet | 2023-02-02 | 2029-10-31 | No | No | Historical |