Allopurinol
- Product NDC
- 55700-947
- 11-digit product format
- 557000947
- Labeler code
- 55700
- Product ID
- 55700-947_5583b017-1bac-4172-afcb-bf279f23930b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2021-09-22
- 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
- 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 |
|---|
| 55700-947-90 | 55700094790 | 90 TABLET in 1 BOTTLE (55700-947-90) | 90 tablet | 2021-09-22 | 0000-00-00 | No | No | Current |