Allopurinol
- Product NDC
- 58118-1156
- 11-digit product format
- 581181156
- Labeler code
- 58118
- Product ID
- 58118-1156_b0136335-797d-5043-e053-2995a90a9e23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA071450
- Marketing category
- ANDA
- Marketing start
- 1987-01-09
- 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 |
|---|
| 58118-1156-8 | 58118115608 | 30 TABLET in 1 BLISTER PACK (58118-1156-8) | 30 tablet | 2018-02-07 | 0000-00-00 | No | No | Current |