Package 72789-305-30

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-305-30
Digits Only 7278930530
Product NDC 72789-305
Product ID 72789-305_4bbc12f8-bd28-29b4-e063-6394a90a2a25
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-305-30)

Marketing

Marketing Status
Marketed Since 2022-03-02
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": "4bbc12f8-bd28-29b4-e063-6394a90a2a25", "openfda": {"upc": ["0372789305301"], "unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["451b8742-8b3c-4335-9075-c1d8313cd3d0"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-305-30)", "package_ndc": "72789-305-30", "marketing_start_date": "20220302"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "72789-305_4bbc12f8-bd28-29b4-e063-6394a90a2a25", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72789-305", "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": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20271231"}