Allopurinol
- Product NDC
- 0615-8321
- 11-digit product format
- 006158321
- Labeler code
- 0615
- Product ID
- 0615-8321_a63c0bcd-b29a-4561-b5e7-69220b1f092f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- NDA018832
- Marketing category
- NDA
- Marketing start
- 2009-04-06
- Marketing end
- 2022-08-31
- Substance
- ALLOPURINOL
- Active strength
- 100 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 |
|---|
| 0615-8321-05 | 00615832105 | 15 TABLET in 1 BLISTER PACK (0615-8321-05) | 15 tablet | 2019-10-03 | 2022-08-31 | No | No | Current |
| 0615-8321-14 | 00615832114 | 14 TABLET in 1 BLISTER PACK (0615-8321-14) | 14 tablet | 2020-05-12 | 2022-08-31 | No | No | Current |
| 0615-8321-39 | 00615832139 | 30 TABLET in 1 BLISTER PACK (0615-8321-39) | 30 tablet | 2019-10-03 | 2022-08-31 | No | No | Current |