Product NDC: | 52959-763 |
Proprietary Name: | ofloxacin |
Non Proprietary Name: | ofloxacin |
Active Ingredient(s): | 3 mg/mL & nbsp; ofloxacin |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52959-763 |
Labeler Name: | H.J. Harkins Company, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078559 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100104 |
Package NDC: | 52959-763-10 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (52959-763-10) > 10 mL in 1 BOTTLE, PLASTIC |
NDC Code | 52959-763-10 |
Proprietary Name | ofloxacin |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (52959-763-10) > 10 mL in 1 BOTTLE, PLASTIC |
Product NDC | 52959-763 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ofloxacin |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20100104 |
Marketing Category Name | ANDA |
Labeler Name | H.J. Harkins Company, Inc. |
Substance Name | OFLOXACIN |
Strength Number | 3 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |