Product NDC: | 0179-0068 |
Proprietary Name: | ANASTROZOLE |
Non Proprietary Name: | ANASTROZOLE |
Active Ingredient(s): | 1 mg/1 & nbsp; ANASTROZOLE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0179-0068 |
Labeler Name: | KAISER FOUNDATION HOSPITALS |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA079220 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100713 |
Package NDC: | 0179-0068-70 |
Package Description: | 30 TABLET in 1 BOX, UNIT-DOSE (0179-0068-70) |
NDC Code | 0179-0068-70 |
Proprietary Name | ANASTROZOLE |
Package Description | 30 TABLET in 1 BOX, UNIT-DOSE (0179-0068-70) |
Product NDC | 0179-0068 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ANASTROZOLE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100713 |
Marketing Category Name | ANDA |
Labeler Name | KAISER FOUNDATION HOSPITALS |
Substance Name | ANASTROZOLE |
Strength Number | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA] |