Allopurinol
- Product NDC
- 43353-501
- 11-digit product format
- 433530501
- Labeler code
- 43353
- Product ID
- 43353-501_8d93d4a2-8f24-4df0-a068-d49234766c97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA078253
- Marketing category
- ANDA
- Marketing start
- 2009-11-16
- Marketing end
- 0000-00-00
- Substance
- ALLOPURINOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 43353-501-60 | 43353050160 | 90 TABLET in 1 BOTTLE (43353-501-60) | 90 tablet | 2022-11-15 | 0000-00-00 | No | No | Current |
| 43353-501-80 | 43353050180 | 180 TABLET in 1 BOTTLE (43353-501-80) | 180 tablet | 2022-11-15 | 0000-00-00 | No | No | Current |