Allopurinol
- Product NDC
- 16714-041
- 11-digit product format
- 167140041
- Labeler code
- 16714
- Product ID
- 16714-041_049208c7-7904-4d26-92ac-d78d4179e3ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northstar RxLLC
- Application
- ANDA078253
- Marketing category
- ANDA
- Marketing start
- 2009-11-16
- 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
- 2022-12-31
- 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 |
|---|
| 16714-041-07 | 16714004107 | 30 TABLET in 1 BOTTLE (16714-041-07) | 30 tablet | 2009-11-16 | 0000-00-00 | No | No | Current |
| 16714-041-10 | 16714004110 | 100 TABLET in 1 BOTTLE (16714-041-10) | 100 tablet | 2009-11-16 | 0000-00-00 | No | No | Current |
| 16714-041-12 | 16714004112 | 1000 TABLET in 1 BOTTLE (16714-041-12) | 1000 tablet | 2009-11-16 | 0000-00-00 | No | No | Current |