Allopurinol
- Product NDC
- 63629-1675
- 11-digit product format
- 636291675
- Labeler code
- 63629
- Product ID
- 63629-1675_b520bdea-fa12-40db-9805-77de6619220d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018832
- Marketing category
- NDA
- Marketing start
- 2009-04-06
- 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 |
|---|
| 63629-1675-1 | 63629167501 | 100 TABLET in 1 BOTTLE (63629-1675-1) | 100 tablet | 2009-04-06 | 0000-00-00 | No | No | Current |
| 63629-1675-2 | 63629167502 | 30 TABLET in 1 BOTTLE (63629-1675-2) | 30 tablet | 2009-04-06 | 0000-00-00 | No | No | Current |
| 63629-1675-3 | 63629167503 | 60 TABLET in 1 BOTTLE (63629-1675-3) | 60 tablet | 2009-04-06 | 0000-00-00 | No | No | Current |
| 63629-1675-4 | 63629167504 | 120 TABLET in 1 BOTTLE (63629-1675-4) | 120 tablet | 2009-04-06 | 0000-00-00 | No | No | Current |
| 63629-1675-5 | 63629167505 | 20 TABLET in 1 BOTTLE (63629-1675-5) | 20 tablet | 2009-04-06 | 0000-00-00 | No | No | Current |
| 63629-1675-6 | 63629167506 | 90 TABLET in 1 BOTTLE (63629-1675-6) | 90 tablet | 2009-04-06 | 0000-00-00 | No | No | Current |