Allopurinol
- Product NDC
- 50090-0044
- 11-digit product format
- 500900044
- Labeler code
- 50090
- Product ID
- 50090-0044_eef4126e-685d-422b-b42f-cf7b154d063b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078253
- Marketing category
- ANDA
- Marketing start
- 2009-11-16
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0044-0 | 50090004400 | 100 TABLET in 1 BOTTLE (50090-0044-0) | 100 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0044-1 | 50090004401 | 30 TABLET in 1 BOTTLE (50090-0044-1) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0044-3 | 50090004403 | 90 TABLET in 1 BOTTLE (50090-0044-3) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |