Cefdinir
- Product NDC
- 70934-062
- 11-digit product format
- 709340062
- Labeler code
- 70934
- Product ID
- 70934-062_d22ea409-2e98-c5ab-e053-2a95a90ad9a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA065434
- Marketing category
- ANDA
- Marketing start
- 2018-01-08
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR
- Active strength
- 300 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 |
|---|
| 70934-062-20 | 70934006220 | 20 CAPSULE in 1 BOTTLE, PLASTIC (70934-062-20) | 20 capsule | 2018-01-08 | 0000-00-00 | No | No | Current |
| 70934-062-30 | 70934006230 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-062-30) | 30 capsule | 2020-03-26 | 0000-00-00 | No | No | Current |