Package 42794-004-02

Brand: protriptyline hydrochloride

Generic: protriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42794-004-02
Digits Only 4279400402
Product NDC 42794-004
Product ID 42794-004_f1f190da-554e-55cb-e053-2a95a90a2871
Description

100 TABLET, FILM COATED in 1 BOTTLE (42794-004-02)

Marketing

Marketing Status
Marketed Since 2020-03-02
Brand protriptyline hydrochloride
Generic protriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Protriptyline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f1f190da-554e-55cb-e053-2a95a90a2871", "openfda": {"upc": ["0342794007026", "0342794004025"], "unii": ["44665V00O8"], "rxcui": ["905168", "905172"], "spl_set_id": ["a023e637-bee9-8c86-e053-2a95a90aa488"], "manufacturer_name": ["Sigmapharm Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42794-004-02)", "package_ndc": "42794-004-02", "marketing_start_date": "20200302"}], "brand_name": "Protriptyline Hydrochloride", "product_id": "42794-004_f1f190da-554e-55cb-e053-2a95a90a2871", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "42794-004", "generic_name": "Protriptyline Hydrochloride", "labeler_name": "Sigmapharm Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Protriptyline Hydrochloride", "active_ingredients": [{"name": "PROTRIPTYLINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090462", "marketing_category": "ANDA", "marketing_start_date": "20200302", "listing_expiration_date": "20261231"}