Cefuroxime Axetil
- Product NDC
- 50090-6999
- 11-digit product format
- 500906999
- Labeler code
- 50090
- Product ID
- 50090-6999_13ec0bb9-d5aa-4e86-91e2-3be896570a4d
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cefuroxime Axetil
- Listing expiration
- 2026-12-31
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 |
|---|
| 50090-6999-0 | Cefuroxime Axetil | 20 in 1 BOTTLE | TABLET | 20 | | 3 |
| 50090-6999-1 | Cefuroxime Axetil | 14 in 1 BOTTLE | TABLET | 14 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6999 | CEFUROXIME AXETIL TABLET [A-S MEDICATION SOLUTIONS] | 3 | Current NDC, 2 package rows | 20240105_bcf7870a-7e45-4ae1-a9b4-457e4781886a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6999-0 | 50090699900 | 20 TABLET in 1 BOTTLE (50090-6999-0) | 20 tablet | 2023-12-27 | No | No | Current |
| 50090-6999-1 | 50090699901 | 14 TABLET in 1 BOTTLE (50090-6999-1) | 14 tablet | 2024-01-03 | No | No | Current |