Cefdinir
- Product NDC
- 71205-183
- 11-digit product format
- 712050183
- Labeler code
- 71205
- Product ID
- 71205-183_3139eb2a-bd08-4fc6-bcf0-28e99f234c43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065337
- Marketing category
- ANDA
- Marketing start
- 2007-04-06
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR
- Active strength
- 250 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-183 | CEFDINIR POWDER, FOR SUSPENSION [PROFICIENT RX LP] | 2 | Legacy NDC | 20191015_5c30c376-e985-433c-8ac9-4c513b4820d8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-183-60 | 71205018360 | 60 mL in 1 BOTTLE (71205-183-60) | 60 ml | 2018-12-01 | 0000-00-00 | No | No | Current |