Allopurinol
- Product NDC
- 0904-7041
- 11-digit product format
- 009047041
- Labeler code
- 0904
- Product ID
- 0904-7041_f28649ef-e682-414b-bebf-f67b15765ac5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA210117
- Marketing category
- ANDA
- Marketing start
- 2018-02-08
- Substance
- ALLOPURINOL
- Active strength
- 100 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Allopurinol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLOPURINOL | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 63CZ7GJN5I |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-7041-61 | Allopurinol | 100 in 1 CARTON | TABLET | 100 | | 5 |
| 0904-7041-61 | Allopurinol | 1 in 1 BLISTER PACK | TABLET | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7041 | ALLOPURINOL TABLET [MAJOR PHARMACEUTICALS] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250209_b630c1cb-d4b7-4f80-b252-5947c1887def.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 |
|---|
| 0904-7041-61 | 00904704161 | 100 BLISTER PACK in 1 CARTON (0904-7041-61) / 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2018-02-08 | 0000-00-00 | No | No | Current |