Product NDC: | 42254-122 |
Proprietary Name: | Ciprofloxacin |
Non Proprietary Name: | Ciprofloxacin |
Active Ingredient(s): | 3 mg/mL & nbsp; Ciprofloxacin |
Administration Route(s): | OPHTHALMIC; TOPICAL |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42254-122 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076673 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050121 |
Package NDC: | 42254-122-05 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (42254-122-05) > 5 mL in 1 BOTTLE, DROPPER |
NDC Code | 42254-122-05 |
Proprietary Name | Ciprofloxacin |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (42254-122-05) > 5 mL in 1 BOTTLE, DROPPER |
Product NDC | 42254-122 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ciprofloxacin |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC; TOPICAL |
Start Marketing Date | 20050121 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
Strength Number | 3 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |