| Product NDC: | 60505-0560 |
| Proprietary Name: | Ofloxacin Ophthalmic |
| 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: | 60505-0560 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076513 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040514 |
| Package NDC: | 60505-0560-1 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (60505-0560-1) > 10 mL in 1 BOTTLE, DROPPER |
| NDC Code | 60505-0560-1 |
| Proprietary Name | Ofloxacin Ophthalmic |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (60505-0560-1) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 60505-0560 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ofloxacin |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20040514 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | OFLOXACIN |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |