CEFUROXIME AXETIL
- Product NDC
- 61919-044
- 11-digit product format
- 619190044
- Labeler code
- 61919
- Product ID
- 61919-044_9c5b1bc4-fa6f-10c6-e053-2995a90a9e9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFUROXIME AXETIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA065308
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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
- 2021-12-31
- 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 |
|---|
| 61919-044-20 | CEFUROXIME AXETIL | 20 in 1 BOTTLE | TABLET | 20 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-044 | CEFUROXIME AXETIL TABLET [DIRECT RX] | 3 | Legacy NDC, 1 package rows | 20200118_82d6ef8a-29cc-4bfb-8801-fdb8fd6f1ff8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-044-20 | 61919004420 | 20 TABLET in 1 BOTTLE (61919-044-20) | 20 tablet | 2015-01-01 | 0000-00-00 | No | No | Current |