Package 63629-2227-1
Brand: midodrine hydrochloride
Generic: midodrine hydrochloridePackage Facts
Identity
Package NDC
63629-2227-1
Digits Only
6362922271
Product NDC
63629-2227
Description
100 TABLET in 1 BOTTLE (63629-2227-1)
Marketing
Marketing Status
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": "eeb7ab44-53b0-47d6-b23f-badbebb8b231", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993466"], "spl_set_id": ["5a6705af-bb72-4edb-863a-93a351bd6dba"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-2227-1)", "package_ndc": "63629-2227-1", "marketing_start_date": "20210322"}], "brand_name": "Midodrine Hydrochloride", "product_id": "63629-2227_eeb7ab44-53b0-47d6-b23f-badbebb8b231", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "63629-2227", "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": "ANDA207169", "marketing_category": "ANDA", "marketing_start_date": "20181029", "listing_expiration_date": "20261231"}