Allopurinol
- Product NDC
- 43063-793
- 11-digit product format
- 430630793
- Labeler code
- 43063
- Product ID
- 43063-793_e69a3950-3f4e-30f5-e053-2a95a90aee48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA018832
- Marketing category
- NDA
- Marketing start
- 2009-04-06
- 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 |
|---|
| 43063-793-20 | 43063079320 | 20 TABLET in 1 BOTTLE, PLASTIC (43063-793-20) | 20 tablet | 2017-10-24 | 0000-00-00 | No | No | Current |
| 43063-793-60 | 43063079360 | 60 TABLET in 1 BOTTLE, PLASTIC (43063-793-60) | 60 tablet | 2017-10-24 | 0000-00-00 | No | No | Current |
| 43063-793-90 | 43063079390 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-793-90) | 90 tablet | 2017-10-06 | 0000-00-00 | No | No | Current |