Package 72162-2560-1
Brand: midodrine hydrochloride
Generic: midodrine hydrochloridePackage Facts
Identity
Package NDC
72162-2560-1
Digits Only
7216225601
Product NDC
72162-2560
Description
100 TABLET in 1 BOTTLE (72162-2560-1)
Marketing
Marketing Status
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": "94fb650d-3ad7-4447-b17e-c6ac262f27d0", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993466"], "spl_set_id": ["db4b18d6-68f9-4d7c-9230-40b928cf859c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2560-1)", "package_ndc": "72162-2560-1", "marketing_start_date": "20251104"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72162-2560_94fb650d-3ad7-4447-b17e-c6ac262f27d0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72162-2560", "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": "ANDA212774", "marketing_category": "ANDA", "marketing_start_date": "20200810", "listing_expiration_date": "20261231"}