Package 0378-1902-01

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0378-1902-01
Digits Only 0378190201
Product NDC 0378-1902
Product ID 0378-1902_e92f278e-0a58-49e3-8fc0-3a16b8474d3b
Description

100 TABLET in 1 BOTTLE, PLASTIC (0378-1902-01)

Marketing

Marketing Status
Marketed Since 2003-09-11
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": "e92f278e-0a58-49e3-8fc0-3a16b8474d3b", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["32fad00b-7e7b-4d35-9e8b-fdc979fdb88e"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0378-1902-01)", "package_ndc": "0378-1902-01", "marketing_start_date": "20030911"}], "brand_name": "Midodrine Hydrochloride", "product_id": "0378-1902_e92f278e-0a58-49e3-8fc0-3a16b8474d3b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0378-1902", "generic_name": "midodrine hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076577", "marketing_category": "ANDA", "marketing_start_date": "20030911", "listing_expiration_date": "20261231"}