Cefdinir
- Product NDC
- 70934-343
- 11-digit product format
- 709340343
- Labeler code
- 70934
- Product ID
- 70934-343_d2419434-e870-da02-e053-2a95a90a7944
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA065264
- Marketing category
- ANDA
- Marketing start
- 2019-04-10
- 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 |
|---|
| 70934-343-20 | 70934034320 | 20 CAPSULE in 1 BOTTLE, PLASTIC (70934-343-20) | 20 capsule | 2019-04-10 | 0000-00-00 | No | No | Current |