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ANASTROZOLE
ANASTROZOLE - 62756-250-88 - (ANASTROZOLE)
Drug Information of ANASTROZOLE
| Product NDC: | 62756-250 |
| Proprietary Name: | ANASTROZOLE |
| Non Proprietary Name: | ANASTROZOLE |
| Active Ingredient(s): | 1 mg/1 & nbsp; ANASTROZOLE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ANASTROZOLE
| Product NDC: | 62756-250 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091177 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100716 |
Package Information of ANASTROZOLE
| Package NDC: | 62756-250-88 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (62756-250-88) |
NDC Information of ANASTROZOLE
| NDC Code | 62756-250-88 |
| Proprietary Name | ANASTROZOLE |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (62756-250-88) |
| Product NDC | 62756-250 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ANASTROZOLE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100716 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | ANASTROZOLE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA] |
