Cefuroxime axetil
- Product NDC
- 55700-655
- 11-digit product format
- 557000655
- Labeler code
- 55700
- Product ID
- 55700-655_fddc413b-41d2-4ccc-99e8-70231e6fcbe8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefuroxime axetil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA065496
- Marketing category
- ANDA
- Marketing start
- 2018-07-13
- Marketing end
- 2021-10-31
- Substance
- CEFUROXIME AXETIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-655-20 | 55700065520 | 20 TABLET, FILM COATED in 1 BOTTLE (55700-655-20) | 2018-07-13 | 0000-00-00 | No | No | Current |