Allopurinol
- Product NDC
- 70934-209
- 11-digit product format
- 709340209
- Labeler code
- 70934
- Product ID
- 70934-209_a56445af-14b2-bfb6-e053-2995a90af71f
- 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
- 2018-12-18
- 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 |
|---|
| 70934-209-30 | 70934020930 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-209-30) | 30 tablet | 2018-12-18 | 0000-00-00 | No | No | Current |
| 70934-209-90 | 70934020990 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-209-90) | 90 tablet | 2020-04-21 | 0000-00-00 | No | No | Current |