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) |
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 NDC: | 0065-0656-10 |
Package Description: | 10 mL in 1 BOTTLE, PLASTIC (0065-0656-10) |
NDC Code | 0065-0656-10 |
Proprietary Name | Ciloxan |
Package Description | 10 mL in 1 BOTTLE, PLASTIC (0065-0656-10) |
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] |