Package 52536-162-01

Brand: perphenazine

Generic: perphenazine
NDC Package

Package Facts

Identity

Package NDC 52536-162-01
Digits Only 5253616201
Product NDC 52536-162
Description

100 TABLET, FILM COATED in 1 BOTTLE (52536-162-01)

Marketing

Marketing Status
Marketed Since 2018-02-06
Brand perphenazine
Generic perphenazine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "325b0584-e6f3-f087-e063-6394a90a64c5", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198075", "198076", "198077", "198078"], "spl_set_id": ["5e455842-4892-4795-8c9b-4109a8f30783"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Wilshire Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (52536-162-01)", "package_ndc": "52536-162-01", "marketing_start_date": "20180206"}], "brand_name": "Perphenazine", "product_id": "52536-162_325b0584-e6f3-f087-e063-6394a90a64c5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "52536-162", "generic_name": "Perphenazine", "labeler_name": "Wilshire Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "2 mg/1"}], "application_number": "ANDA205973", "marketing_category": "ANDA", "marketing_start_date": "20180206", "listing_expiration_date": "20261231"}