Allopurinol
- Product NDC
- 55700-879
- 11-digit product format
- 557000879
- Labeler code
- 55700
- Product ID
- 55700-879_c35aa65c-4e7c-4aba-9a78-0f99a0506328
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA071586
- Marketing category
- ANDA
- Marketing start
- 2020-08-19
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-879-90 | 55700087990 | 90 TABLET in 1 BOTTLE (55700-879-90) | 90 tablet | 2020-08-19 | 0000-00-00 | No | No | Current |