CEFUROXIME AXETIL
- Product NDC
- 61919-747
- 11-digit product format
- 619190747
- Labeler code
- 61919
- Product ID
- 61919-747_f215a829-30cf-b78d-e053-2a95a90a7ac7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFUROXIME AXETIL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA065496
- Marketing category
- ANDA
- Marketing start
- 2019-08-13
- 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| Z49QDT0J8Z | CEFUROXIME AXETIL | 64544-07-6 | CEFUROXIME AXETIL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-747-20 | 61919074720 | 20 TABLET, FILM COATED in 1 BOTTLE (61919-747-20) | 2019-08-13 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| CEFUROXIME AXETIL | Direct_Rx | 2023-01-12 | HUMAN PRESCRIPTION DRUG LABEL | 2 |