Allopurinol
- Product NDC
- 60429-180
- 11-digit product format
- 604290180
- Labeler code
- 60429
- Product ID
- 60429-180_9b7d7e1d-6463-1596-e053-2995a90ab361
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA071586
- Marketing category
- ANDA
- Marketing start
- 1987-04-02
- 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 |
|---|
| 60429-180-18 | 60429018018 | 180 TABLET in 1 BOTTLE (60429-180-18) | 180 tablet | 2015-02-20 | 0000-00-00 | No | No | Current |