Allopurinol
- Product NDC
- 70934-295
- 11-digit product format
- 709340295
- Labeler code
- 70934
- Product ID
- 70934-295_b7b3ac60-dec6-fd5f-e053-2a95a90a307d
- 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
- 2019-02-25
- 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 |
|---|
| 70934-295-30 | 70934029530 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-295-30) | 30 tablet | 2019-02-25 | 0000-00-00 | No | No | Current |
| 70934-295-90 | 70934029590 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-295-90) | 90 tablet | 2019-06-10 | 0000-00-00 | No | No | Current |