Allopurinol
- Product NDC
- 50090-5194
- 11-digit product format
- 500905194
- Labeler code
- 50090
- Product ID
- 50090-5194_e9b58ec3-f8fc-4d0e-b09f-d699aff7213c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALLOPURINOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2015-04-29
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5194 | ALLOPURINOL TABLET [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC | 20240417_5fe03530-5659-4359-bdf9-d752c2f5272f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5194-0 | 50090519400 | 100 TABLET in 1 BOTTLE (50090-5194-0) | 100 tablet | 2020-09-30 | 0000-00-00 | No | No | Current |
| 50090-5194-1 | 50090519401 | 30 TABLET in 1 BOTTLE (50090-5194-1) | 30 tablet | 2020-09-30 | 0000-00-00 | No | No | Current |
| 50090-5194-3 | 50090519403 | 90 TABLET in 1 BOTTLE (50090-5194-3) | 90 tablet | 2020-09-30 | 0000-00-00 | No | No | Current |