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LETROZOLE
LETROZOLE - 51991-759-10 - (LETROZOLE)
Drug Information of LETROZOLE
| Product NDC: | 51991-759 |
| Proprietary Name: | LETROZOLE |
| Non Proprietary Name: | LETROZOLE |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; LETROZOLE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LETROZOLE
| Product NDC: | 51991-759 |
| Labeler Name: | Breckenridge Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200161 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110604 |
Package Information of LETROZOLE
| Package NDC: | 51991-759-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (51991-759-10) |
NDC Information of LETROZOLE
| NDC Code | 51991-759-10 |
| Proprietary Name | LETROZOLE |
| Package Description | 1000 TABLET in 1 BOTTLE (51991-759-10) |
| Product NDC | 51991-759 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LETROZOLE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110604 |
| Marketing Category Name | ANDA |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| Substance Name | LETROZOLE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA] |
