Allopurinol
- Product NDC
- 63739-796
- 11-digit product format
- 637390796
- Labeler code
- 63739
- Product ID
- 63739-796_e8414cac-ff5d-5af4-e053-2995a90a2e95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA078253
- Marketing category
- ANDA
- Marketing start
- 2009-11-16
- 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
- 2023-12-31
- 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 |
|---|
| 63739-796-10 | 63739079610 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-796-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2017-03-08 | 0000-00-00 | No | No | Current |