Package 85293-005-01

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 85293-005-01
Digits Only 8529300501
Product NDC 85293-005
Product ID 85293-005_2fb355a4-09cf-880d-e063-6394a90a8178
Description

100 TABLET in 1 BOTTLE (85293-005-01)

Marketing

Marketing Status
Marketed Since 2025-03-05
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": "2fb355a4-09cf-880d-e063-6394a90a8178", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["4f5e1689-9691-471b-a39c-26120d6ce073"], "manufacturer_name": ["Umasuto, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (85293-005-01)", "package_ndc": "85293-005-01", "marketing_start_date": "20250305"}], "brand_name": "Midodrine Hydrochloride", "product_id": "85293-005_2fb355a4-09cf-880d-e063-6394a90a8178", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "85293-005", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Umasuto, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA207613", "marketing_category": "ANDA", "marketing_start_date": "20250305", "listing_expiration_date": "20261231"}