Package 71335-2171-1

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2171-1
Digits Only 7133521711
Product NDC 71335-2171
Product ID 71335-2171_16f050fb-b3b9-4907-a67c-63642ff31f0e
Description

30 TABLET in 1 BOTTLE (71335-2171-1)

Marketing

Marketing Status
Marketed Since 2023-04-14
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": "16f050fb-b3b9-4907-a67c-63642ff31f0e", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993470"], "spl_set_id": ["60d5a132-9cfc-48e2-aa71-1949aeb255c3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2171-1)", "package_ndc": "71335-2171-1", "marketing_start_date": "20230414"}], "brand_name": "Midodrine Hydrochloride", "product_id": "71335-2171_16f050fb-b3b9-4907-a67c-63642ff31f0e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "71335-2171", "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": "5 mg/1"}], "application_number": "ANDA212543", "marketing_category": "ANDA", "marketing_start_date": "20190819", "listing_expiration_date": "20261231"}