Package 50268-562-15

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-562-15
Digits Only 5026856215
Product NDC 50268-562
Product ID 50268-562_32fa2977-8701-5efb-e063-6394a90a2dff
Description

50 TABLET in 1 BOX (50268-562-15)

Marketing

Marketing Status
Marketed Since 2019-08-26
Brand midodrine hydrochloride
Generic midodrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Midodrine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "32fa2977-8701-5efb-e063-6394a90a2dff", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["9106776e-601a-4e3c-e053-2995a90a5435"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOX (50268-562-15)", "package_ndc": "50268-562-15", "marketing_start_date": "20190826"}], "brand_name": "Midodrine Hydrochloride", "product_id": "50268-562_32fa2977-8701-5efb-e063-6394a90a2dff", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "50268-562", "generic_name": "Midodrine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077746", "marketing_category": "ANDA", "marketing_start_date": "20190826", "listing_expiration_date": "20261231"}