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Cipro
Cipro - 54868-4365-0 - (ciprofloxacin hydrochloride, hydrocortisone and benzyl alcohol)
Drug Information of Cipro
| Product NDC: | 54868-4365 |
| Proprietary Name: | Cipro |
| Non Proprietary Name: | ciprofloxacin hydrochloride, hydrocortisone and benzyl alcohol |
| Active Ingredient(s): | 9; 2; 10 mg/mL; mg/mL; mg/mL & nbsp; ciprofloxacin hydrochloride, hydrocortisone and benzyl alcohol |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cipro
| Product NDC: | 54868-4365 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020805 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090212 |
Package Information of Cipro
| Package NDC: | 54868-4365-0 |
| Package Description: | 10 mL in 1 BOTTLE, GLASS (54868-4365-0) |
NDC Information of Cipro
| NDC Code | 54868-4365-0 |
| Proprietary Name | Cipro |
| Package Description | 10 mL in 1 BOTTLE, GLASS (54868-4365-0) |
| Product NDC | 54868-4365 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ciprofloxacin hydrochloride, hydrocortisone and benzyl alcohol |
| Dosage Form Name | SUSPENSION |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20090212 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | BENZYL ALCOHOL; CIPROFLOXACIN HYDROCHLORIDE; HYDROCORTISONE |
| Strength Number | 9; 2; 10 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Pediculicide [EPC] |
