Product NDC: | 21695-990 |
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: | 21695-990 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA079220 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100701 |
Package NDC: | 21695-990-30 |
Package Description: | 30 TABLET in 1 BOTTLE (21695-990-30) |
NDC Code | 21695-990-30 |
Proprietary Name | Anastrozole |
Package Description | 30 TABLET in 1 BOTTLE (21695-990-30) |
Product NDC | 21695-990 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Anastrozole |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100701 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | ANASTROZOLE |
Strength Number | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA] |