ALLOPURINOL
- Product NDC
- 70518-4404
- 11-digit product format
- 705184404
- Labeler code
- 70518
- Product ID
- 70518-4404_4a142f8c-ee72-cae7-e063-6294a90ad762
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALLOPURINOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA217748
- Marketing category
- ANDA
- Marketing start
- 2025-07-26
- 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 | 197320 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4404-0 | ALLOPURINOL | 30 in 1 BLISTER PACK | TABLET | 30 | | 2 |
| 70518-4404-1 | ALLOPURINOL | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4404-0 | 70518440400 | 30 TABLET in 1 BLISTER PACK (70518-4404-0) | 30 tablet | 2025-07-26 | No | No | Historical |
| 70518-4404-1 | 70518440401 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-4404-1) | 100 tablet | 2026-02-05 | No | No | Historical |