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Flurbiprofen Sodium
Flurbiprofen Sodium - 24208-314-25 - (Flurbiprofen Sodium)
Drug Information of Flurbiprofen Sodium
| Product NDC: | 24208-314 |
| Proprietary Name: | Flurbiprofen Sodium |
| Non Proprietary Name: | Flurbiprofen Sodium |
| Active Ingredient(s): | .3 mg/mL & nbsp; Flurbiprofen Sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flurbiprofen Sodium
| Product NDC: | 24208-314 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074447 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950104 |
Package Information of Flurbiprofen Sodium
| Package NDC: | 24208-314-25 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-314-25) > 2.5 mL in 1 BOTTLE, DROPPER |
NDC Information of Flurbiprofen Sodium
| NDC Code | 24208-314-25 |
| Proprietary Name | Flurbiprofen Sodium |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-314-25) > 2.5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-314 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flurbiprofen Sodium |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19950104 |
| Marketing Category Name | ANDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | FLURBIPROFEN SODIUM |
| Strength Number | .3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
