Allopurinol
- Product NDC
- 70934-072
- 11-digit product format
- 709340072
- Labeler code
- 70934
- Product ID
- 70934-072_ae4636e0-e0ef-fe85-e053-2995a90a2570
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2019-10-24
- 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
- 2021-12-31
- 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 |
|---|
| 70934-072-30 | 70934007230 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-072-30) | 30 tablet | 2019-10-24 | 0000-00-00 | No | No | Current |
| 70934-072-90 | 70934007290 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-072-90) | 90 tablet | 2019-10-30 | 0000-00-00 | No | No | Current |