NDC 24208-314
Flurbiprofen Sodium
Flurbiprofen Sodium
Flurbiprofen Sodium is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is Flurbiprofen Sodium.
Product ID | 24208-314_7447bbfb-f922-4866-a9d0-09d469433780 |
NDC | 24208-314 |
Product Type | Human Prescription Drug |
Proprietary Name | Flurbiprofen Sodium |
Generic Name | Flurbiprofen Sodium |
Dosage Form | Solution/ Drops |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 1995-01-04 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA074447 |
Labeler Name | Bausch & Lomb Incorporated |
Substance Name | FLURBIPROFEN SODIUM |
Active Ingredient Strength | 0 mg/mL |
Pharm Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |