Package 72789-465-01

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-465-01
Digits Only 7278946501
Product NDC 72789-465
Description

100 TABLET in 1 BOTTLE, PLASTIC (72789-465-01)

Marketing

Marketing Status
Marketed Since 2024-12-26
Brand midodrine hydrochloride
Generic midodrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e13fe26-c4c4-17ce-e063-6394a90ae0bd", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993466"], "spl_set_id": ["54ded041-c78c-4646-a1cc-c94afcd62690"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-465-01)", "package_ndc": "72789-465-01", "marketing_start_date": "20241226"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-465-90)", "package_ndc": "72789-465-90", "marketing_start_date": "20250905"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72789-465_3e13fe26-c4c4-17ce-e063-6394a90ae0bd", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72789-465", "generic_name": "Midodrine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA212543", "marketing_category": "ANDA", "marketing_start_date": "20190819", "listing_expiration_date": "20261231"}