Product NDC: | 17478-106 |
Proprietary Name: | Levofloxacin |
Non Proprietary Name: | Levofloxacin |
Active Ingredient(s): | 5 mg/mL & nbsp; Levofloxacin |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17478-106 |
Labeler Name: | Akorn Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090268 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110301 |
Package NDC: | 17478-106-10 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-106-10) > 5 mL in 1 BOTTLE, DROPPER |
NDC Code | 17478-106-10 |
Proprietary Name | Levofloxacin |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-106-10) > 5 mL in 1 BOTTLE, DROPPER |
Product NDC | 17478-106 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Levofloxacin |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110301 |
Marketing Category Name | ANDA |
Labeler Name | Akorn Inc. |
Substance Name | LEVOFLOXACIN |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |