Package 70954-538-10

Brand: tranylcypromine

Generic: tranylcypromine
NDC Package

Package Facts

Identity

Package NDC 70954-538-10
Digits Only 7095453810
Product NDC 70954-538
Description

100 TABLET in 1 BOTTLE (70954-538-10)

Marketing

Marketing Status
Marketed Since 2021-06-06
Brand tranylcypromine
Generic tranylcypromine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8ab1c887-76fb-44ca-9999-4eefd3778cfc", "openfda": {"upc": ["0370954538103"], "unii": ["7ZAT6ES870"], "rxcui": ["313447"], "spl_set_id": ["8ab1c887-76fb-44ca-9999-4eefd3778cfc"], "manufacturer_name": ["Novitium Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-538-10)", "package_ndc": "70954-538-10", "marketing_start_date": "20210606"}], "brand_name": "Tranylcypromine", "product_id": "70954-538_8ab1c887-76fb-44ca-9999-4eefd3778cfc", "dosage_form": "TABLET", "pharm_class": ["Monoamine Oxidase Inhibitor [EPC]", "Monoamine Oxidase Inhibitors [MoA]"], "product_ndc": "70954-538", "generic_name": "Tranylcypromine", "labeler_name": "Novitium Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tranylcypromine", "active_ingredients": [{"name": "TRANYLCYPROMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA206856", "marketing_category": "ANDA", "marketing_start_date": "20210606", "listing_expiration_date": "20261231"}