Package 69413-558-40

Brand: vecamyl

Generic: mecamylamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69413-558-40
Digits Only 6941355840
Product NDC 69413-558
Description

100 TABLET in 1 BOTTLE (69413-558-40)

Marketing

Marketing Status
Marketed Since 2013-03-19
Brand vecamyl
Generic mecamylamine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a29db678-f591-44c7-be1c-3ec7ae06bea7", "openfda": {"upc": ["0369413558400"], "unii": ["4956DJR58O"], "rxcui": ["1298874", "1373008"], "spl_set_id": ["0774cc48-7287-4093-91d6-9df41a81408a"], "manufacturer_name": ["Vyera Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69413-558-40)", "package_ndc": "69413-558-40", "marketing_start_date": "20130319"}], "brand_name": "Vecamyl", "product_id": "69413-558_a29db678-f591-44c7-be1c-3ec7ae06bea7", "dosage_form": "TABLET", "pharm_class": ["Autonomic Ganglionic Blocker [EPC]", "Decreased Autonomic Ganglionic Activity [PE]"], "product_ndc": "69413-558", "generic_name": "Mecamylamine Hydrochloride", "labeler_name": "Vyera Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vecamyl", "active_ingredients": [{"name": "MECAMYLAMINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA204054", "marketing_category": "ANDA", "marketing_start_date": "20130319", "listing_expiration_date": "20261231"}