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Bromday
Bromday - 24208-099-01 - (bromfenac)
Drug Information of Bromday
| Product NDC: | 24208-099 |
| Proprietary Name: | Bromday |
| Non Proprietary Name: | bromfenac |
| Active Ingredient(s): | .9 mg/mL & nbsp; bromfenac |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bromday
| Product NDC: | 24208-099 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021664 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100920 |
Package Information of Bromday
| Package NDC: | 24208-099-01 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-099-01) > 1.7 mL in 1 BOTTLE, DROPPER |
NDC Information of Bromday
| NDC Code | 24208-099-01 |
| Proprietary Name | Bromday |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-099-01) > 1.7 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-099 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bromfenac |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20100920 |
| Marketing Category Name | NDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | BROMFENAC SODIUM |
| Strength Number | .9 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
