Cefuroxime axetil
- Product NDC
- 21695-150
- 11-digit product format
- 216950150
- Labeler code
- 21695
- Product ID
- 21695-150_1f35ed70-4947-4d4d-b4c8-71ce520fc445
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefuroxime axetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA065308
- Marketing category
- ANDA
- Marketing start
- 2006-03-29
- Marketing end
- 0000-00-00
- Substance
- CEFUROXIME AXETIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-150-20 | Cefuroxime axetil | 20 in 1 BOTTLE | TABLET | 20 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-150 | CEFUROXIME AXETIL TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20101123_1f35ed70-4947-4d4d-b4c8-71ce520fc445.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-150-20 | 21695015020 | 20 in 1 BOTTLE | Historical |