| 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] |