Cefadroxil
- Product NDC
- 68071-2752
- 11-digit product format
- 680712752
- Labeler code
- 68071
- Product ID
- 68071-2752_e09261c7-1818-3042-e053-2a95a90aef90
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065352
- Marketing category
- ANDA
- Marketing start
- 2007-01-25
- Marketing end
- 0000-00-00
- Substance
- CEFADROXIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 280111G160 | CEFADROXIL | 66592-87-8 | CEFADROXIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2752-1 | 68071275201 | 100 CAPSULE in 1 BOTTLE (68071-2752-1) | 100 capsule | 2022-06-03 | 0000-00-00 | No | No | Current |