Package 64980-435-01

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64980-435-01
Digits Only 6498043501
Product NDC 64980-435
Description

100 TABLET in 1 BOTTLE (64980-435-01)

Marketing

Marketing Status
Marketed Since 2019-04-01
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": "311a8e3c-0112-4c91-a7cc-92709b41f170", "openfda": {"upc": ["0364980435017", "0364980433013", "0364980434010"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["ffd4dfb9-a6d8-4c81-8b8c-8228d9e2f93e"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-435-01)", "package_ndc": "64980-435-01", "marketing_start_date": "20190401"}], "brand_name": "Midodrine Hydrochloride", "product_id": "64980-435_311a8e3c-0112-4c91-a7cc-92709b41f170", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "64980-435", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207613", "marketing_category": "ANDA", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}