Allopurinol
- Product NDC
- 62135-517
- 11-digit product format
- 621350517
- Labeler code
- 62135
- Product ID
- 62135-517_4b432cc5-11c8-4450-e063-6394a90a1053
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA077353
- Marketing category
- ANDA
- Marketing start
- 2006-05-11
- Substance
- ALLOPURINOL
- Active strength
- 300 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 | 300 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 63CZ7GJN5I |
| Rxcui | 197319, 197320 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-517-31 | Allopurinol | 300 in 1 BOTTLE | TABLET | 300 | | 3 |
| 62135-517-90 | 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 |
|---|
| 62135-517 | ALLOPURINOL TABLET [CHARTWELL RX, LLC] | 2 | Current NDC, 2 package rows | 20241127_cdc3f33b-ff2b-4a84-a820-51a497fdf3d9.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 |
|---|
| 62135-517-31 | 62135051731 | 300 TABLET in 1 BOTTLE (62135-517-31) | 300 tablet | 2023-01-27 | No | No | Historical |
| 62135-517-90 | 62135051790 | 90 TABLET in 1 BOTTLE (62135-517-90) | 90 tablet | 2023-01-27 | No | No | Historical |