Package 11788-082-01

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 11788-082-01
Digits Only 1178808201
Product NDC 11788-082
Product ID 11788-082_4ee04ba3-df06-44c2-8476-09b6cd38f863
Description

100 TABLET in 1 BOTTLE (11788-082-01)

Marketing

Marketing Status
Marketed Since 2025-11-01
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": "4ee04ba3-df06-44c2-8476-09b6cd38f863", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["33807ee6-8443-4613-8bbe-d66f6010fc60"], "manufacturer_name": ["AiPing Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (11788-082-01)", "package_ndc": "11788-082-01", "marketing_start_date": "20251101"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "11788-082_4ee04ba3-df06-44c2-8476-09b6cd38f863", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "11788-082", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "AiPing Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA212654", "marketing_category": "ANDA", "marketing_start_date": "20251101", "listing_expiration_date": "20261231"}