Package 63629-2346-1

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2346-1
Digits Only 6362923461
Product NDC 63629-2346
Product ID 63629-2346_8bfa3b96-7a9d-411c-b193-be6de1269691
Description

100 TABLET in 1 BOTTLE, PLASTIC (63629-2346-1)

Marketing

Marketing Status
Marketed Since 2021-04-19
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": "8bfa3b96-7a9d-411c-b193-be6de1269691", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462"], "spl_set_id": ["df43f108-c89c-49e7-9c1a-77a0ce9b03b5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63629-2346-1)", "package_ndc": "63629-2346-1", "marketing_start_date": "20210419"}], "brand_name": "Midodrine Hydrochloride", "product_id": "63629-2346_8bfa3b96-7a9d-411c-b193-be6de1269691", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "63629-2346", "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": "10 mg/1"}], "application_number": "ANDA207849", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}