Cefadroxil
- Product NDC
- 0143-9766
- 11-digit product format
- 001439766
- Labeler code
- 0143
- Product ID
- 0143-9766_ab8f4cac-f079-413d-82b0-cd1b2ef8a8f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA091036
- Marketing category
- ANDA
- Marketing start
- 2012-11-28
- Marketing end
- 0000-00-00
- Substance
- CEFADROXIL
- Active strength
- 500 mg/5mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0143-9766-01 | 00143976601 | 100 mL in 1 BOTTLE (0143-9766-01) | 100 ml | 2012-11-28 | 0000-00-00 | No | No | Current |
| 0143-9766-75 | 00143976675 | 75 mL in 1 BOTTLE (0143-9766-75) | 75 ml | 2012-11-28 | 0000-00-00 | No | No | Current |