Package 81469-141-90

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 81469-141-90
Digits Only 8146914190
Product NDC 81469-141
Product ID 81469-141_6e30fa38-fd26-4d37-a5f4-9e044c383362
Description

90 TABLET in 1 BOTTLE (81469-141-90)

Marketing

Marketing Status
Marketed Since 2025-08-13
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": "6e30fa38-fd26-4d37-a5f4-9e044c383362", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["414cebaa-b87f-4d41-bc41-a77dcd3ea434"], "manufacturer_name": ["First Nation Group, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (81469-141-90)", "package_ndc": "81469-141-90", "marketing_start_date": "20250813"}], "brand_name": "Midodrine Hydrochloride", "product_id": "81469-141_6e30fa38-fd26-4d37-a5f4-9e044c383362", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "81469-141", "generic_name": "Midodrine Hydrochloride", "labeler_name": "First Nation Group, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA217271", "marketing_category": "ANDA", "marketing_start_date": "20250813", "listing_expiration_date": "20261231"}