Febuxostat
- Product NDC
- 69539-036
- 11-digit product format
- 695390036
- Labeler code
- 69539
- Product ID
- 69539-036_778b95e5-ced2-4b08-b0b6-baa7fd82e4ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Febuxostat
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- MSN LABORATORIES PRIVATE LIMITED
- Application
- ANDA210461
- Marketing category
- ANDA
- Marketing start
- 2019-12-30
- Marketing end
- 0000-00-00
- Substance
- FEBUXOSTAT
- Active strength
- 80 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 |
|---|
| 69539-036 | FEBUXOSTAT TABLET, FILM COATED [MSN LABORATORIES PRIVATE LIMITED] | 5 | Legacy NDC | 20230811_b94994e0-cdb5-42cc-bc3c-75154e87561d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69539-036-30 | 69539003630 | 30 TABLET, FILM COATED in 1 BOTTLE (69539-036-30) | 2019-12-30 | 0000-00-00 | No | No | Current |
| 69539-036-91 | 69539003691 | 100 TABLET, FILM COATED in 1 BOTTLE (69539-036-91) | 2019-12-30 | 0000-00-00 | No | No | Current |
| 69539-036-99 | 69539003699 | 1000 TABLET, FILM COATED in 1 BOTTLE (69539-036-99) | 2019-12-30 | 0000-00-00 | No | No | Current |