Allopurinol
- Product NDC
- 60760-134
- 11-digit product format
- 607600134
- Labeler code
- 60760
- Product ID
- 60760-134_f06e6e94-f0e4-7303-e053-2a95a90afa61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2017-12-20
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-134 | ALLOPURINOL TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 4 | Legacy NDC | 20221223_60cdd69c-fd25-77de-e053-2a91aa0ad472.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-134-90 | 60760013490 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-134-90) | 90 tablet | 2017-12-20 | 0000-00-00 | No | No | Current |