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Cefdinir
Cefdinir - 21695-620-20 - (Cefdinir)
Drug Information of Cefdinir
| Product NDC: | 21695-620 |
| Proprietary Name: | Cefdinir |
| Non Proprietary Name: | Cefdinir |
| Active Ingredient(s): | 300 mg/1 & nbsp; Cefdinir |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefdinir
| Product NDC: | 21695-620 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065434 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080107 |
Package Information of Cefdinir
| Package NDC: | 21695-620-20 |
| Package Description: | 20 CAPSULE in 1 BOTTLE (21695-620-20) |
NDC Information of Cefdinir
| NDC Code | 21695-620-20 |
| Proprietary Name | Cefdinir |
| Package Description | 20 CAPSULE in 1 BOTTLE (21695-620-20) |
| Product NDC | 21695-620 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefdinir |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20080107 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CEFDINIR |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
