ALLOPURINOL
- Product NDC
- 71335-2744
- 11-digit product format
- 713352744
- Labeler code
- 71335
- Product ID
- 71335-2744_17448c5c-7701-4767-91f8-238b570e9921
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALLOPURINOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA217748
- Marketing category
- ANDA
- Marketing start
- 2023-08-03
- 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#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2744-1 | 71335274401 | 100 TABLET in 1 BOTTLE (71335-2744-1) | 100 tablet | 2025-10-02 | No | No | Historical |
| 71335-2744-2 | 71335274402 | 30 TABLET in 1 BOTTLE (71335-2744-2) | 30 tablet | 2025-10-02 | No | No | Historical |
| 71335-2744-3 | 71335274403 | 60 TABLET in 1 BOTTLE (71335-2744-3) | 60 tablet | 2025-10-02 | No | No | Historical |
| 71335-2744-4 | 71335274404 | 120 TABLET in 1 BOTTLE (71335-2744-4) | 120 tablet | 2025-10-02 | No | No | Historical |
| 71335-2744-5 | 71335274405 | 20 TABLET in 1 BOTTLE (71335-2744-5) | 20 tablet | 2025-10-02 | No | No | Historical |
| 71335-2744-6 | 71335274406 | 90 TABLET in 1 BOTTLE (71335-2744-6) | 90 tablet | 2025-10-02 | No | No | Historical |