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CIPRODEX
CIPRODEX - 21695-969-75 - (ciprofloxacin and dexamethasone)
Drug Information of CIPRODEX
| Product NDC: | 21695-969 |
| Proprietary Name: | CIPRODEX |
| Non Proprietary Name: | ciprofloxacin and dexamethasone |
| Active Ingredient(s): | 3; 1 mg/mL; mg/mL & nbsp; ciprofloxacin and dexamethasone |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CIPRODEX
| Product NDC: | 21695-969 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021537 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030815 |
Package Information of CIPRODEX
| Package NDC: | 21695-969-75 |
| Package Description: | 7.5 mL in 1 BOTTLE, PLASTIC (21695-969-75) |
NDC Information of CIPRODEX
| NDC Code | 21695-969-75 |
| Proprietary Name | CIPRODEX |
| Package Description | 7.5 mL in 1 BOTTLE, PLASTIC (21695-969-75) |
| Product NDC | 21695-969 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ciprofloxacin and dexamethasone |
| Dosage Form Name | SUSPENSION |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20030815 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE; DEXAMETHASONE |
| Strength Number | 3; 1 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
