Cefuroxime axetil
- Product NDC
- 63629-9448
- 11-digit product format
- 636299448
- Labeler code
- 63629
- Product ID
- 63629-9448_7043e0ff-48ca-4778-aa65-c97d0258d0d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefuroxime axetil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065496
- Marketing category
- ANDA
- Marketing start
- 2010-12-01
- Marketing end
- 0000-00-00
- Substance
- CEFUROXIME AXETIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- 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 |
|---|
| 63629-9448 | CEFUROXIME AXETIL TABLET, FILM COATED [BRYANT RANCH PREPACK] | 101 | Legacy NDC | 20230317_aa1c5720-b698-415f-997f-cbe4e35c69be.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-9448-1 | 63629944801 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-9448-1) | 2022-09-28 | 0000-00-00 | No | No | Current |