Package 72603-607-01

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-607-01
Digits Only 7260360701
Product NDC 72603-607
Product ID 72603-607_3370f087-6bac-2032-e063-6394a90a9a60
Description

100 TABLET in 1 BOTTLE (72603-607-01)

Marketing

Marketing Status
Marketed Since 2025-04-21
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": "3370f087-6bac-2032-e063-6394a90a9a60", "openfda": {"upc": ["0372603606010", "0372603605013", "0372603607017"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["b015c98f-57e6-410b-9c9d-8898aa22082a"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-607-01)", "package_ndc": "72603-607-01", "marketing_start_date": "20250421"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72603-607_3370f087-6bac-2032-e063-6394a90a9a60", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72603-607", "generic_name": "Midodrine Hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA212543", "marketing_category": "ANDA", "marketing_start_date": "20250421", "listing_expiration_date": "20261231"}