Package 72162-2066-2

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2066-2
Digits Only 7216220662
Product NDC 72162-2066
Product ID 72162-2066_3ea72e38-318d-4702-ac31-ee0a5275eb24
Description

120 TABLET in 1 BOTTLE (72162-2066-2)

Marketing

Marketing Status
Marketed Since 2023-08-15
Brand cyproheptadine hydrochloride
Generic cyproheptadine hydrochloride
Sample Package No

Linked Drug Pages (1)

CYPROHEPTADINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ea72e38-318d-4702-ac31-ee0a5275eb24", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["1bfb14ad-b522-4ad6-8c9f-2d99dd0dce64"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2066-0)", "package_ndc": "72162-2066-0", "marketing_start_date": "20230815"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2066-1)", "package_ndc": "72162-2066-1", "marketing_start_date": "20230815"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (72162-2066-2)", "package_ndc": "72162-2066-2", "marketing_start_date": "20230815"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-2066-9)", "package_ndc": "72162-2066-9", "marketing_start_date": "20230815"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "72162-2066_3ea72e38-318d-4702-ac31-ee0a5275eb24", "dosage_form": "TABLET", "product_ndc": "72162-2066", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA212491", "marketing_category": "ANDA", "marketing_start_date": "20210224", "listing_expiration_date": "20261231"}