Package 52817-210-50

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 52817-210-50
Digits Only 5281721050
Product NDC 52817-210
Product ID 52817-210_c67264ab-9491-4aee-a28a-c97e1497915b
Description

500 TABLET in 1 BOTTLE, PLASTIC (52817-210-50)

Marketing

Marketing Status
Marketed Since 2017-01-17
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": "c67264ab-9491-4aee-a28a-c97e1497915b", "openfda": {"upc": ["0352817210500", "0352817210104"], "unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["9c0b47c0-ecd2-450f-9dcb-c262db92866e"], "manufacturer_name": ["TRUPHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (52817-210-10)", "package_ndc": "52817-210-10", "marketing_start_date": "20170117"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (52817-210-50)", "package_ndc": "52817-210-50", "marketing_start_date": "20170117"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "52817-210_c67264ab-9491-4aee-a28a-c97e1497915b", "dosage_form": "TABLET", "product_ndc": "52817-210", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "TRUPHARMA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA206553", "marketing_category": "ANDA", "marketing_start_date": "20170117", "listing_expiration_date": "20261231"}