Allopurinol
- Product NDC
- 63629-8020
- 11-digit product format
- 636298020
- Labeler code
- 63629
- Product ID
- 63629-8020_d2f86cad-4a6b-443e-9fcf-f721a9565383
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2015-04-29
- 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 |
|---|
| 63629-8020-1 | 63629802001 | 90 TABLET in 1 BOTTLE (63629-8020-1) | 90 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |