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Ciloxan
Ciloxan - 0065-0656-25 - (ciprofloxacin hydrochloride)
Drug Information of Ciloxan
| Product NDC: | 0065-0656 |
| Proprietary Name: | Ciloxan |
| Non Proprietary Name: | ciprofloxacin hydrochloride |
| Active Ingredient(s): | 3.5 mg/mL & nbsp; ciprofloxacin hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciloxan
| Product NDC: | 0065-0656 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019992 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19910115 |
Package Information of Ciloxan
| Package NDC: | 0065-0656-25 |
| Package Description: | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0656-25) |
NDC Information of Ciloxan
| NDC Code | 0065-0656-25 |
| Proprietary Name | Ciloxan |
| Package Description | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0656-25) |
| Product NDC | 0065-0656 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ciprofloxacin hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19910115 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | 3.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
