Package 72162-1973-1

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1973-1
Digits Only 7216219731
Product NDC 72162-1973
Product ID 72162-1973_89d34db8-3963-42bf-8f9a-91b0354f951e
Description

100 TABLET in 1 BOTTLE, PLASTIC (72162-1973-1)

Marketing

Marketing Status
Marketed Since 2024-02-07
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": "89d34db8-3963-42bf-8f9a-91b0354f951e", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993466"], "spl_set_id": ["9c1ccd24-3f9c-489c-9fd2-98e69531d5ab"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1973-1)", "package_ndc": "72162-1973-1", "marketing_start_date": "20240207"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72162-1973_89d34db8-3963-42bf-8f9a-91b0354f951e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72162-1973", "generic_name": "midodrine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA207849", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}