Zyloprim
- Product NDC
- 70199-032
- 11-digit product format
- 701990032
- Labeler code
- 70199
- Product ID
- 70199-032_a78bda09-7bbe-413b-b192-b0b76e0194f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Casper Pharma LLC
- Application
- NDA016084
- Marketing category
- NDA
- Marketing start
- 2022-08-04
- Marketing end
- 0000-00-00
- Substance
- ALLOPURINOL
- Active strength
- 200 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70199-032-01 | 70199003201 | 100 TABLET in 1 BOTTLE (70199-032-01) | 100 tablet | 2022-08-04 | 0000-00-00 | No | No | Current |
| 70199-032-05 | 70199003205 | 500 TABLET in 1 BOTTLE (70199-032-05) | 500 tablet | 2022-08-04 | 0000-00-00 | No | No | Current |
| 70199-032-90 | 70199003290 | 90 TABLET in 1 BOTTLE (70199-032-90) | 90 tablet | 2022-08-04 | 0000-00-00 | No | No | Current |
| 70199-032-99 | 70199003299 | 1000 TABLET in 1 BOTTLE (70199-032-99) | 1000 tablet | 2022-08-04 | 0000-00-00 | No | No | Current |