Package 0078-0249-15

Brand: femara

Generic: letrozole
NDC Package

Package Facts

Identity

Package NDC 0078-0249-15
Digits Only 0078024915
Product NDC 0078-0249
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0078-0249-15)

Marketing

Marketing Status
Marketed Since 1997-07-31
Brand femara
Generic letrozole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f052c25a-d848-4b2d-8ff3-73bee0c89ad7", "openfda": {"nui": ["N0000175563", "N0000175080"], "unii": ["7LKK855W8I"], "rxcui": ["153124", "200064"], "spl_set_id": ["82b77d74-085f-45ac-a7dd-1f5c038bf406"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0078-0249-15)", "package_ndc": "0078-0249-15", "marketing_start_date": "19970731"}], "brand_name": "Femara", "product_id": "0078-0249_f052c25a-d848-4b2d-8ff3-73bee0c89ad7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "0078-0249", "generic_name": "letrozole", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Femara", "active_ingredients": [{"name": "LETROZOLE", "strength": "2.5 mg/1"}], "application_number": "NDA020726", "marketing_category": "NDA", "marketing_start_date": "19970731", "listing_expiration_date": "20261231"}