Package 43063-822-30

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-822-30
Digits Only 4306382230
Product NDC 43063-822
Product ID 43063-822_39fa3a63-d264-557f-e063-6294a90a8630
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-822-30)

Marketing

Marketing Status
Marketed Since 2018-01-08
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": "39fa3a63-d264-557f-e063-6294a90a8630", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["1523a2b4-f9d6-4d3c-a370-df579ed36911"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-822-30)", "package_ndc": "43063-822-30", "marketing_start_date": "20180108"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "43063-822_39fa3a63-d264-557f-e063-6294a90a8630", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "43063-822", "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": "25 mg/1"}], "application_number": "ANDA085968", "marketing_category": "ANDA", "marketing_start_date": "19771121", "listing_expiration_date": "20261231"}