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Flurbiprofen
Flurbiprofen - 55289-561-60 - (flurbiprofen)
Drug Information of Flurbiprofen
| Product NDC: | 55289-561 |
| Proprietary Name: | Flurbiprofen |
| Non Proprietary Name: | flurbiprofen |
| Active Ingredient(s): | 100 mg/1 & nbsp; flurbiprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flurbiprofen
| Product NDC: | 55289-561 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074358 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110520 |
Package Information of Flurbiprofen
| Package NDC: | 55289-561-60 |
| Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-561-60) |
NDC Information of Flurbiprofen
| NDC Code | 55289-561-60 |
| Proprietary Name | Flurbiprofen |
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-561-60) |
| Product NDC | 55289-561 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | flurbiprofen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110520 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | FLURBIPROFEN |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
