Allopurinol
- Product NDC
- 50090-6715
- 11-digit product format
- 500906715
- Labeler code
- 50090
- Product ID
- 50090-6715_442dbea1-5257-4621-b47d-44844c0d9e3e
- 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
- 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
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLOPURINOL | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 63CZ7GJN5I |
| Rxcui | 197319 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6715-3 | Allopurinol | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 50090-6715-4 | Allopurinol | 90 in 1 BOTTLE | TABLET | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6715 | ALLOPURINOL TABLET [A-S MEDICATION SOLUTIONS] | 4 | Current NDC, 2 package rows | 20241226_74dba96f-d388-40fe-8bca-53086d28c954.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6715-3 | 50090671503 | 30 TABLET in 1 BOTTLE (50090-6715-3) | 30 tablet | 2023-10-05 | No | No | Current |
| 50090-6715-4 | 50090671504 | 90 TABLET in 1 BOTTLE (50090-6715-4) | 90 tablet | 2023-10-05 | No | No | Current |