Package 71921-190-33
Brand: exemestane
Generic: exemestanePackage Facts
Identity
Package NDC
71921-190-33
Digits Only
7192119033
Product NDC
71921-190
Description
30 TABLET, FILM COATED in 1 BOTTLE (71921-190-33)
Marketing
Marketing Status
Brand
exemestane
Generic
exemestane
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "28c7c528-d203-40c9-a06f-cbe4b0d73326", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0371921190331"], "unii": ["NY22HMQ4BX"], "rxcui": ["310261"], "spl_set_id": ["9354d1a1-8e8c-4c6a-b7ad-d4fe14b10a8b"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71921-190-33)", "package_ndc": "71921-190-33", "marketing_start_date": "20210115"}], "brand_name": "Exemestane", "product_id": "71921-190_28c7c528-d203-40c9-a06f-cbe4b0d73326", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "71921-190", "generic_name": "Exemestane", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Exemestane", "active_ingredients": [{"name": "EXEMESTANE", "strength": "25 mg/1"}], "application_number": "ANDA213547", "marketing_category": "ANDA", "marketing_start_date": "20210115", "listing_expiration_date": "20261231"}