Allopurinol
- Product NDC
- 70518-4062
- 11-digit product format
- 705184062
- Labeler code
- 70518
- Product ID
- 70518-4062_3fa2ab4e-8412-51e6-e063-6394a90a8e5d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204467
- Marketing category
- ANDA
- Marketing start
- 2024-05-04
- 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 |
|---|
| 70518-4062-0 | Allopurinol | 30 in 1 BLISTER PACK | TABLET | 30 | | 4 |
| 70518-4062-1 | Allopurinol | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-4062 | ALLOPURINOL TABLET [REMEDYREPACK INC.] | 2 | Current NDC, 2 package rows | 20240726_165f2ebb-a099-4d31-b21a-93b341c39429.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 |
|---|
| 70518-4062-0 | 70518406200 | 30 in 1 BLISTER PACK | | | | | Historical |
| 70518-4062-1 | 70518406201 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-4062-1) | 90 tablet | 2024-06-07 | No | No | Current |