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OCUFLOX
OCUFLOX - 11980-779-05 - (ofloxacin)
Drug Information of OCUFLOX
| Product NDC: | 11980-779 |
| Proprietary Name: | OCUFLOX |
| Non Proprietary Name: | ofloxacin |
| Active Ingredient(s): | 3 mg/mL & nbsp; ofloxacin |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OCUFLOX
| Product NDC: | 11980-779 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019921 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930801 |
Package Information of OCUFLOX
| Package NDC: | 11980-779-05 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (11980-779-05) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of OCUFLOX
| NDC Code | 11980-779-05 |
| Proprietary Name | OCUFLOX |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (11980-779-05) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 11980-779 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ofloxacin |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19930801 |
| Marketing Category Name | NDA |
| Labeler Name | Allergan, Inc. |
| Substance Name | OFLOXACIN |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
