Allopurinol
- Product NDC
- 49999-374
- 11-digit product format
- 499990374
- Labeler code
- 49999
- Product ID
- 49999-374_414be1f1-302b-423a-9c15-3ad660b623be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- NDA018877
- Marketing category
- NDA
- Marketing start
- 2010-04-01
- Marketing end
- 2021-04-30
- Substance
- ALLOPURINOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 49999-374-30 | 49999037430 | 30 TABLET in 1 BOTTLE, PLASTIC (49999-374-30) | 30 tablet | 2010-04-01 | 2021-04-30 | No | No | Current |
| 49999-374-90 | 49999037490 | 90 TABLET in 1 BOTTLE, PLASTIC (49999-374-90) | 90 tablet | 2010-04-01 | 2021-04-30 | No | No | Current |