Package 71335-1433-1

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1433-1
Digits Only 7133514331
Product NDC 71335-1433
Product ID 71335-1433_e9091702-8e76-49a1-8ea7-6612c792fd0e
Description

30 TABLET in 1 BOTTLE (71335-1433-1)

Marketing

Marketing Status
Marketed Since 2019-12-10
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": "e9091702-8e76-49a1-8ea7-6612c792fd0e", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993470"], "spl_set_id": ["c41f7ec2-a3d7-4ff0-b51d-feda49717e7b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1433-1)", "package_ndc": "71335-1433-1", "marketing_start_date": "20191210"}], "brand_name": "Midodrine Hydrochloride", "product_id": "71335-1433_e9091702-8e76-49a1-8ea7-6612c792fd0e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "71335-1433", "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": "5 mg/1"}], "application_number": "ANDA077746", "marketing_category": "ANDA", "marketing_start_date": "20060912", "listing_expiration_date": "20261231"}