Allopurinol
- Product NDC
- 70934-389
- 11-digit product format
- 709340389
- Labeler code
- 70934
- Product ID
- 70934-389_af48c5d4-9183-e871-e053-2995a90ab4d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA071450
- Marketing category
- ANDA
- Marketing start
- 2019-06-05
- 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
- 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 |
|---|
| 70934-389-30 | 70934038930 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-389-30) | 30 tablet | 2019-07-17 | 0000-00-00 | No | No | Current |
| 70934-389-90 | 70934038990 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-389-90) | 90 tablet | 2019-06-05 | 0000-00-00 | No | No | Current |