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Bromfenac
Bromfenac - 0378-7111-35 - (Bromfenac sodium)
Drug Information of Bromfenac
| Product NDC: | 0378-7111 |
| Proprietary Name: | Bromfenac |
| Non Proprietary Name: | Bromfenac sodium |
| Active Ingredient(s): | .9 mg/mL & nbsp; Bromfenac sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bromfenac
| Product NDC: | 0378-7111 |
| Labeler Name: | Mylan Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201211 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110511 |
Package Information of Bromfenac
| Package NDC: | 0378-7111-35 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0378-7111-35) > 2.5 mL in 1 BOTTLE, DROPPER |
NDC Information of Bromfenac
| NDC Code | 0378-7111-35 |
| Proprietary Name | Bromfenac |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0378-7111-35) > 2.5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0378-7111 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Bromfenac sodium |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110511 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals, Inc. |
| 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] |
