Cefdinir
- Product NDC
- 50090-1034
- 11-digit product format
- 500901034
- Labeler code
- 50090
- Product ID
- 50090-1034_8cf05412-1927-4fc0-a9f4-bbf7eeec6967
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065264
- Marketing category
- ANDA
- Marketing start
- 2006-05-30
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1034-0 | 50090103400 | 20 CAPSULE in 1 BOTTLE (50090-1034-0) | 20 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |