Allopurinol
- Product NDC
- 70518-1678
- 11-digit product format
- 705181678
- Labeler code
- 70518
- Product ID
- 70518-1678_c3cdf66c-07d4-18c4-e053-2a95a90a9742
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018832
- Marketing category
- NDA
- Marketing start
- 2018-11-19
- 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
- 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 |
|---|
| 70518-1678 | ALLOPURINOL TABLET [REMEDYREPACK INC.] | 6 | Legacy NDC | 20210603_51f0a5a5-74d6-4d98-9338-c518d5d4a334.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1678-1 | 70518167801 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1678-1) | 90 tablet | 2018-12-13 | 0000-00-00 | No | No | Current |