Package 70756-202-11

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70756-202-11
Digits Only 7075620211
Product NDC 70756-202
Product ID 70756-202_197990ae-46aa-4a70-b5f5-bb47f74acf9f
Description

100 TABLET, FILM COATED in 1 BOTTLE (70756-202-11)

Marketing

Marketing Status
Marketed Since 2021-02-23
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": "197990ae-46aa-4a70-b5f5-bb47f74acf9f", "openfda": {"upc": ["0370756203124", "0370756206118"], "unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["67e31675-1da2-4acf-84ac-77522b02f0b9"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70756-202-11)", "package_ndc": "70756-202-11", "marketing_start_date": "20210223"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (70756-202-12)", "package_ndc": "70756-202-12", "marketing_start_date": "20210223"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70756-202_197990ae-46aa-4a70-b5f5-bb47f74acf9f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70756-202", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA213999", "marketing_category": "ANDA", "marketing_start_date": "20210223", "listing_expiration_date": "20271231"}