Cefadroxil
- Product NDC
- 0143-9948
- 11-digit product format
- 001439948
- Labeler code
- 0143
- Product ID
- 0143-9948_c99bebb5-e9ce-48ce-9e2e-62d69f5e082e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA065260
- Marketing category
- ANDA
- Marketing start
- 2006-03-30
- Marketing end
- 0000-00-00
- Substance
- CEFADROXIL
- Active strength
- 1 g/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0143-9948-01 | 00143994801 | 100 TABLET, FILM COATED in 1 BOTTLE (0143-9948-01) | 2006-03-30 | 0000-00-00 | No | No | Current |
| 0143-9948-50 | 00143994850 | 50 TABLET, FILM COATED in 1 BOTTLE (0143-9948-50) | 2006-03-30 | 0000-00-00 | No | No | Current |