Allopurinol
- Product NDC
- 71335-2542
- 11-digit product format
- 713352542
- Labeler code
- 71335
- Product ID
- 71335-2542_6056bc9e-a945-4876-85be-d4cff7e03411
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA214443
- Marketing category
- ANDA
- Marketing start
- 2024-05-01
- 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 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2542-1 | 71335254201 | 100 TABLET in 1 BOTTLE (71335-2542-1) | 100 tablet | 2024-12-10 | No | No | Historical |
| 71335-2542-2 | 71335254202 | 30 TABLET in 1 BOTTLE (71335-2542-2) | 30 tablet | 2024-12-10 | No | No | Historical |
| 71335-2542-3 | 71335254203 | 60 TABLET in 1 BOTTLE (71335-2542-3) | 60 tablet | 2024-12-10 | No | No | Historical |
| 71335-2542-4 | 71335254204 | 120 TABLET in 1 BOTTLE (71335-2542-4) | 120 tablet | 2024-12-10 | No | No | Historical |
| 71335-2542-5 | 71335254205 | 20 TABLET in 1 BOTTLE (71335-2542-5) | 20 tablet | 2024-12-10 | No | No | Historical |
| 71335-2542-6 | 71335254206 | 90 TABLET in 1 BOTTLE (71335-2542-6) | 90 tablet | 2024-12-10 | No | No | Historical |