Package 0781-1489-01

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0781-1489-01
Digits Only 0781148901
Product NDC 0781-1489
Product ID 0781-1489_9df45420-7268-454e-9624-8da48c97b7db
Description

100 TABLET, FILM COATED in 1 BOTTLE (0781-1489-01)

Marketing

Marketing Status
Marketed Since 1977-11-29
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": "9df45420-7268-454e-9624-8da48c97b7db", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["705a2bae-031d-4218-82fe-4346542c0baa"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-1489-01)", "package_ndc": "0781-1489-01", "marketing_start_date": "19771129"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "0781-1489_9df45420-7268-454e-9624-8da48c97b7db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0781-1489", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA085968", "marketing_category": "ANDA", "marketing_start_date": "19771129", "listing_expiration_date": "20261231"}