Package 59762-0119-1

Brand: phenelzine sulfate

Generic: phenelzine sulfate
NDC Package

Package Facts

Identity

Package NDC 59762-0119-1
Digits Only 5976201191
Product NDC 59762-0119
Description

60 TABLET, FILM COATED in 1 BOTTLE (59762-0119-1)

Marketing

Marketing Status
Marketed Since 2011-03-23
Brand phenelzine sulfate
Generic phenelzine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a1789800-9bb6-42d3-967f-122f07c5b69c", "openfda": {"upc": ["0359762011916"], "unii": ["2681D7P965"], "rxcui": ["312347"], "spl_set_id": ["fa041652-fdde-4794-a8d2-279dd309e075"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (59762-0119-1)", "package_ndc": "59762-0119-1", "marketing_start_date": "20110323"}], "brand_name": "phenelzine sulfate", "product_id": "59762-0119_a1789800-9bb6-42d3-967f-122f07c5b69c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Monoamine Oxidase Inhibitor [EPC]", "Monoamine Oxidase Inhibitors [MoA]"], "product_ndc": "59762-0119", "generic_name": "Phenelzine Sulfate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "phenelzine sulfate", "active_ingredients": [{"name": "PHENELZINE SULFATE", "strength": "15 mg/1"}], "application_number": "NDA011909", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20110323", "listing_expiration_date": "20261231"}