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Bicalutamide
Bicalutamide - 51079-692-03 - (bicalutamide)
Drug Information of Bicalutamide
| Product NDC: | 51079-692 |
| Proprietary Name: | Bicalutamide |
| Non Proprietary Name: | bicalutamide |
| Active Ingredient(s): | 50 mg/1 & nbsp; bicalutamide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bicalutamide
| Product NDC: | 51079-692 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079185 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091030 |
Package Information of Bicalutamide
| Package NDC: | 51079-692-03 |
| Package Description: | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-692-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-692-01) |
NDC Information of Bicalutamide
| NDC Code | 51079-692-03 |
| Proprietary Name | Bicalutamide |
| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-692-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-692-01) |
| Product NDC | 51079-692 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bicalutamide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091030 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | BICALUTAMIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Androgen Receptor Antagonists [MoA],Androgen Receptor Inhibitor [EPC] |
