Zyloprim
- Product NDC
- 67046-681
- 11-digit product format
- 670460681
- Labeler code
- 67046
- Product ID
- 67046-681_65171cf0-8487-1ca6-e053-2991aa0ab91f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA018659
- Marketing category
- ANDA
- Marketing start
- 2018-02-23
- 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
- 2020-12-31
- 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 |
|---|
| 67046-681 | ZYLOPRIM (ALLOPURINOL) TABLET [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC | 20180224_65171cf0-8486-1ca6-e053-2991aa0ab91f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67046-681-30 | 67046068130 | 30 TABLET in 1 BLISTER PACK (67046-681-30) | 30 tablet | 2018-02-23 | 0000-00-00 | No | No | Current |