Allopurinol
- Product NDC
- 70518-1573
- 11-digit product format
- 705181573
- Labeler code
- 70518
- Product ID
- 70518-1573_c32c2857-6537-62d5-e053-2995a90a766e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018877
- Marketing category
- NDA
- Marketing start
- 2018-10-22
- Marketing end
- 0000-00-00
- Substance
- ALLOPURINOL
- Active strength
- 300 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1573-0 | 70518157300 | 30 TABLET in 1 BLISTER PACK (70518-1573-0) | 30 tablet | 2018-10-22 | 0000-00-00 | No | No | Current |
| 70518-1573-1 | 70518157301 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-1573-1) | 100 tablet | 2019-01-22 | 0000-00-00 | No | No | Current |
| 70518-1573-2 | 70518157302 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1573-2) | 90 tablet | 2019-07-10 | 0000-00-00 | No | No | Current |