Cefuroxime Axetil
- Product NDC
- 55700-436
- 11-digit product format
- 557000436
- Labeler code
- 55700
- Product ID
- 55700-436_3d845541-eecc-45e6-88b7-43bf3fb9bd09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefuroxime Axetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA065308
- Marketing category
- ANDA
- Marketing start
- 2006-03-29
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-436-20 | 55700043620 | 20 TABLET in 1 BOTTLE (55700-436-20) | 20 tablet | 2016-10-03 | 2021-10-31 | No | No | Current |