Cefdinir
- Product NDC
- 16714-392
- 11-digit product format
- 167140392
- Labeler code
- 16714
- Product ID
- 16714-392_88c96697-7f83-4497-81aa-a93c95a7a444
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA065473
- Marketing category
- ANDA
- Marketing start
- 2007-12-14
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR
- Active strength
- 125 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-392-01 | 16714039201 | 1 BOTTLE in 1 CARTON (16714-392-01) > 60 mL in 1 BOTTLE | 1 bottle | 2007-12-14 | 0000-00-00 | No | No | Current |
| 16714-392-02 | 16714039202 | 1 BOTTLE in 1 CARTON (16714-392-02) > 100 mL in 1 BOTTLE | 1 bottle | 2007-12-14 | 0000-00-00 | No | No | Current |