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
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 |
|---|
| 61919-747-20 | CEFUROXIME AXETIL | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-747 | CEFUROXIME AXETIL TABLET, FILM COATED [DIRECT_RX] | 2 | Legacy NDC, 1 package rows | 20230113_90001905-36e4-b0e1-e053-2995a90a4d93.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 |