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Anastrozole
Anastrozole - 0781-5356-31 - (Anastrozole)
Drug Information of Anastrozole
| Product NDC: | 0781-5356 |
| 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: | 0781-5356 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079007 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100628 |
Package Information of Anastrozole
| Package NDC: | 0781-5356-31 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5356-31) |
NDC Information of Anastrozole
| NDC Code | 0781-5356-31 |
| Proprietary Name | Anastrozole |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5356-31) |
| Product NDC | 0781-5356 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Anastrozole |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100628 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | ANASTROZOLE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA] |
