Cefadroxil
- Product NDC
- 70518-2538
- 11-digit product format
- 705182538
- Labeler code
- 70518
- Product ID
- 70518-2538_dc258d5e-f636-16f7-e053-2995a90a47fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065352
- Marketing category
- ANDA
- Marketing start
- 2020-01-11
- 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
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-2538-0 | 70518253800 | 30 CAPSULE in 1 BLISTER PACK (70518-2538-0) | 30 capsule | 2020-01-11 | 0000-00-00 | No | No | Current |
| 70518-2538-1 | 70518253801 | 20 CAPSULE in 1 BLISTER PACK (70518-2538-1) | 20 capsule | 2020-01-17 | 0000-00-00 | No | No | Current |