CEFADROXIL
- Product NDC
- 72189-103
- 11-digit product format
- 721890103
- Labeler code
- 72189
- Product ID
- 72189-103_2be86c94-8c9d-1da3-e063-6294a90a1319
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFADROXIL
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA065352
- Marketing category
- ANDA
- Marketing start
- 2020-06-12
- Substance
- CEFADROXIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 72189-103-06 | 72189010306 | 6 CAPSULE in 1 BOTTLE (72189-103-06) | 6 capsule | 2020-06-12 | No | No | Historical |
| 72189-103-20 | 72189010320 | 20 CAPSULE in 1 BOTTLE (72189-103-20) | 20 capsule | 2020-06-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| CEFADROXIL | DIRECT RX | 2025-01-17 | HUMAN PRESCRIPTION DRUG LABEL | 4 |