Package 68382-738-01

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68382-738-01
Digits Only 6838273801
Product NDC 68382-738
Product ID 68382-738_fe679311-db62-4004-800d-2961962340de
Description

100 TABLET in 1 BOTTLE (68382-738-01)

Marketing

Marketing Status
Marketed Since 2020-09-17
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": "fe679311-db62-4004-800d-2961962340de", "openfda": {"upc": ["0368382739018"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["3bc97210-fa2f-4979-abdf-d92e5973e6e3"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-738-01)", "package_ndc": "68382-738-01", "marketing_start_date": "20200917"}], "brand_name": "Midodrine hydrochloride", "product_id": "68382-738_fe679311-db62-4004-800d-2961962340de", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "68382-738", "generic_name": "Midodrine hydrochloride", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA213055", "marketing_category": "ANDA", "marketing_start_date": "20200917", "listing_expiration_date": "20261231"}