Package 71335-3037-1

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-3037-1
Digits Only 7133530371
Product NDC 71335-3037
Product ID 71335-3037_aaaed4a4-358b-4f58-82ce-1ea0213f9fad
Description

100 TABLET in 1 BOTTLE (71335-3037-1)

Marketing

Marketing Status
Marketed Since 2025-12-03
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": "aaaed4a4-358b-4f58-82ce-1ea0213f9fad", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993466"], "spl_set_id": ["78d447cb-e3ff-433b-9758-b907a75b0666"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-3037-1)", "package_ndc": "71335-3037-1", "marketing_start_date": "20251203"}], "brand_name": "Midodrine Hydrochloride", "product_id": "71335-3037_aaaed4a4-358b-4f58-82ce-1ea0213f9fad", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "71335-3037", "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"}