Package 71205-823-30

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-823-30
Digits Only 7120582330
Product NDC 71205-823
Product ID 71205-823_0221f0ce-11e7-171c-e063-6294a90af405
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-823-30)

Marketing

Marketing Status
Marketed Since 2023-08-01
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": "0221f0ce-11e7-171c-e063-6294a90af405", "openfda": {"upc": ["0371205823306"], "unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["e42225f5-44bd-451e-98a1-aa3877457733"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-823-30)", "package_ndc": "71205-823-30", "marketing_start_date": "20230801"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-823-60)", "package_ndc": "71205-823-60", "marketing_start_date": "20230801"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-823-90)", "package_ndc": "71205-823-90", "marketing_start_date": "20230801"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "71205-823_0221f0ce-11e7-171c-e063-6294a90af405", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71205-823", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}