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Flarex
Flarex - 0065-0096-05 - (fluorometholone acetate)
Drug Information of Flarex
| Product NDC: | 0065-0096 |
| Proprietary Name: | Flarex |
| Non Proprietary Name: | fluorometholone acetate |
| Active Ingredient(s): | 1 mg/mL & nbsp; fluorometholone acetate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flarex
| Product NDC: | 0065-0096 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019079 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19920206 |
Package Information of Flarex
| Package NDC: | 0065-0096-05 |
| Package Description: | 5 mL in 1 BOTTLE, PLASTIC (0065-0096-05) |
NDC Information of Flarex
| NDC Code | 0065-0096-05 |
| Proprietary Name | Flarex |
| Package Description | 5 mL in 1 BOTTLE, PLASTIC (0065-0096-05) |
| Product NDC | 0065-0096 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluorometholone acetate |
| Dosage Form Name | SUSPENSION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19920206 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | FLUOROMETHOLONE ACETATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
