Package 51991-005-90

Brand: exemestane

Generic: exemestane
NDC Package

Package Facts

Identity

Package NDC 51991-005-90
Digits Only 5199100590
Product NDC 51991-005
Product ID 51991-005_cb46b87b-4bbc-4aed-8656-877a480061af
Description

90 TABLET, FILM COATED in 1 BOTTLE (51991-005-90)

Marketing

Marketing Status
Marketed Since 2020-11-15
Brand exemestane
Generic exemestane
Sample Package No

Linked Drug Pages (1)

Exemestane ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cb46b87b-4bbc-4aed-8656-877a480061af", "openfda": {"nui": ["N0000175563", "N0000175080"], "unii": ["NY22HMQ4BX"], "rxcui": ["310261"], "spl_set_id": ["4e3fd382-19f5-4ded-ab22-39d5b1b2f366"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Breckenridge Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (51991-005-90)", "package_ndc": "51991-005-90", "marketing_start_date": "20201115"}], "brand_name": "Exemestane", "product_id": "51991-005_cb46b87b-4bbc-4aed-8656-877a480061af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "51991-005", "generic_name": "Exemestane", "labeler_name": "Breckenridge Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Exemestane", "active_ingredients": [{"name": "EXEMESTANE", "strength": "25 mg/1"}], "application_number": "ANDA211031", "marketing_category": "ANDA", "marketing_start_date": "20191219", "listing_expiration_date": "20261231"}