Package 50742-190-01

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50742-190-01
Digits Only 5074219001
Product NDC 50742-190
Product ID 50742-190_4357bb59-3551-49fd-8fcf-2d90c801776a
Description

100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01)

Marketing

Marketing Status
Marketed Since 2015-09-23
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": "4357bb59-3551-49fd-8fcf-2d90c801776a", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["56f428c9-8d33-4c91-91d8-1fe194335066"], "manufacturer_name": ["Ingenus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01)", "package_ndc": "50742-190-01", "marketing_start_date": "20150923"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10)", "package_ndc": "50742-190-10", "marketing_start_date": "20150923"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "50742-190_4357bb59-3551-49fd-8fcf-2d90c801776a", "dosage_form": "TABLET", "product_ndc": "50742-190", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Ingenus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA205087", "marketing_category": "ANDA", "marketing_start_date": "20150923", "listing_expiration_date": "20261231"}