Cefuroxime Axetil
- Product NDC
- 64679-921
- 11-digit product format
- 646790921
- Labeler code
- 64679
- Product ID
- 64679-921_46ecfa55-090f-42a2-9671-a7028c3521fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefuroxime Axetil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA065166
- Marketing category
- ANDA
- Marketing start
- 2005-07-29
- Marketing end
- 0000-00-00
- Substance
- CEFUROXIME AXETIL
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64679-921-01 | 64679092101 | 20 TABLET, FILM COATED in 1 BOTTLE (64679-921-01) | 2005-07-29 | 0000-00-00 | No | No | Current |
| 64679-921-02 | 64679092102 | 60 TABLET, FILM COATED in 1 BOTTLE (64679-921-02) | 2005-07-29 | 0000-00-00 | No | No | Current |