Allopurinol
- Product NDC
- 70518-0451
- 11-digit product format
- 705180451
- Labeler code
- 70518
- Product ID
- 70518-0451_eb5260e1-d973-44f0-e053-2995a90a9eee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2017-04-21
- 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 |
|---|
| 70518-0451 | ALLOPURINOL TABLET [REMEDYREPACK INC.] | 22 | Legacy NDC | 20250427_c6c33885-7d24-4029-bba1-66dbfa45c8a0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0451-0 | 70518045100 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0451-0) | 90 tablet | 2017-04-21 | 0000-00-00 | No | No | Current |
| 70518-0451-1 | 70518045101 | 30 TABLET in 1 BLISTER PACK (70518-0451-1) | 30 tablet | 2019-11-29 | 0000-00-00 | No | No | Current |
| 70518-0451-2 | 70518045102 | 10 TABLET in 1 BLISTER PACK (70518-0451-2) | 10 tablet | 2020-12-07 | 0000-00-00 | No | No | Current |
| 70518-0451-3 | 70518045103 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-0451-3) | 180 tablet | 2021-11-12 | 0000-00-00 | No | No | Current |
| 70518-0451-4 | 70518045104 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-0451-4) | 30 tablet | 2022-01-31 | 0000-00-00 | No | No | Current |