Allopurinol
- Product NDC
- 70518-1806
- 11-digit product format
- 705181806
- Labeler code
- 70518
- Product ID
- 70518-1806_ea265518-a050-a801-e053-2a95a90a65d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALLOPURINOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2019-01-18
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1806 | ALLOPURINOL TABLET [REMEDYREPACK INC.] | 13 | Legacy NDC | 20250228_82b83653-a097-464d-8265-672aba502aa8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1806-0 | 70518180600 | 30 TABLET in 1 BLISTER PACK (70518-1806-0) | 30 tablet | 2019-01-18 | 0000-00-00 | No | No | Current |
| 70518-1806-1 | 70518180601 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1806-1) | 90 tablet | 2020-06-16 | 0000-00-00 | No | No | Current |
| 70518-1806-2 | 70518180602 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-1806-2) | 100 tablet | 2020-09-01 | 0000-00-00 | No | No | Current |