Zyloprim
- Product NDC
- 70199-015
- 11-digit product format
- 701990015
- Labeler code
- 70199
- Product ID
- 70199-015_c014e234-aeb6-4ada-ae8b-97791ff3c923
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Casper Pharma LLC
- Application
- NDA016084
- Marketing category
- NDA
- Marketing start
- 2018-08-06
- 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
- 2020-12-31
- 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 |
|---|
| 70199-015-90 | 70199001590 | 90 TABLET in 1 BOTTLE (70199-015-90) | 90 tablet | 2018-08-06 | 0000-00-00 | No | No | Current |