Package 43063-836-30

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-836-30
Digits Only 4306383630
Product NDC 43063-836
Product ID 43063-836_39fa6955-dc56-8a30-e063-6294a90abf8e
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-836-30)

Marketing

Marketing Status
Marketed Since 2018-02-14
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Amitriptyline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39fa6955-dc56-8a30-e063-6294a90abf8e", "openfda": {"upc": ["0343063836309"], "unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["d7bfeb47-2482-4217-b522-df4444499133"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-836-30)", "package_ndc": "43063-836-30", "marketing_start_date": "20180214"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "43063-836_39fa6955-dc56-8a30-e063-6294a90abf8e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "43063-836", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA085968", "marketing_category": "ANDA", "marketing_start_date": "19771129", "listing_expiration_date": "20261231"}