Cefadroxil
- Product NDC
- 70934-056
- 11-digit product format
- 709340056
- Labeler code
- 70934
- Product ID
- 70934-056_d22e897b-0da2-64d0-e053-2995a90a7055
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA065352
- Marketing category
- ANDA
- Marketing start
- 2017-12-28
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-056-20 | 70934005620 | 20 CAPSULE in 1 BOTTLE, PLASTIC (70934-056-20) | 20 capsule | 2019-03-20 | 0000-00-00 | No | No | Current |
| 70934-056-91 | 70934005691 | 20 CAPSULE in 1 DOSE PACK (70934-056-91) | 20 capsule | 2017-12-28 | 0000-00-00 | No | No | Current |
| 70934-056-94 | 70934005694 | 30 CAPSULE in 1 DOSE PACK (70934-056-94) | 30 capsule | 2017-12-28 | 0000-00-00 | No | No | Current |