Allopurinol
- Product NDC
- 62584-713
- 11-digit product format
- 625840713
- Labeler code
- 62584
- Product ID
- 62584-713_f038b51e-2b8a-2249-e053-2a95a90ae5c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- NDA018877
- Marketing category
- NDA
- Marketing start
- 2004-02-27
- Marketing end
- 2023-10-31
- Substance
- ALLOPURINOL
- Active strength
- 300 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 62584-713-01 | 62584071301 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (62584-713-01) > 1 TABLET in 1 BLISTER PACK (62584-713-11) | 100 blister pack | 2004-02-27 | 0000-00-00 | No | No | Current |