Cefuroxime Axetil
- Product NDC
- 50090-7667
- 11-digit product format
- 500907667
- Labeler code
- 50090
- Product ID
- 50090-7667_d122394a-0bd4-412c-b87b-46f66b761914
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefuroxime Axetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065308
- Marketing category
- ANDA
- Marketing start
- 2006-03-29
- Substance
- CEFUROXIME AXETIL
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cefuroxime Axetil
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEFUROXIME AXETIL | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Z49QDT0J8Z |
| Rxcui | 309097 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7667-0 | Cefuroxime Axetil | 20 in 1 BOTTLE | TABLET | 20 | | 3 |
| 50090-7667-1 | Cefuroxime Axetil | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7667-0 | 50090766700 | 20 TABLET in 1 BOTTLE (50090-7667-0) | 20 tablet | 2025-10-06 | No | No | Current |
| 50090-7667-1 | 50090766701 | 60 TABLET in 1 BOTTLE (50090-7667-1) | 60 tablet | 2025-10-06 | No | No | Current |