Allopurinol
- Product NDC
- 55700-540
- 11-digit product format
- 557000540
- Labeler code
- 55700
- Product ID
- 55700-540_9836cf2b-322b-4f5f-8aff-4a0f8c47cbd7
- 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
- 2017-08-11
- Marketing end
- 0000-00-00
- Substance
- ALLOPURINOL
- Active strength
- 300 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 |
|---|
| 55700-540-30 | 55700054030 | 30 TABLET in 1 BOTTLE, PLASTIC (55700-540-30) | 30 tablet | 2017-08-11 | 0000-00-00 | No | No | Current |
| 55700-540-90 | 55700054090 | 90 TABLET in 1 BOTTLE, PLASTIC (55700-540-90) | 90 tablet | 2017-08-11 | 0000-00-00 | No | No | Current |