midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: umasuto, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler umasuto, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 2.5 mg/1

Manufacturer
Umasuto, LLC

Identifiers & Regulatory

Product NDC 85293-005
Product ID 85293-005_2fb355a4-09cf-880d-e063-6394a90a8178
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207613
Listing Expiration 2026-12-31
Marketing Start 2025-03-05

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 85293005
Hyphenated Format 85293-005

Supplemental Identifiers

RxCUI
993462 993466 993470
UNII
59JV96YTXV

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name midodrine hydrochloride (source: ndc)
Generic Name midodrine hydrochloride (source: ndc)
Application Number ANDA207613 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (85293-005-01)
source: ndc

Packages (1)

85293-005-01 100 TABLET in 1 BOTTLE (85293-005-01)

Ingredients (1)

midodrine hydrochloride (2.5 mg/1)

Linked Drug Pages (1)

Midodrine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2fb355a4-09cf-880d-e063-6394a90a8178", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["4f5e1689-9691-471b-a39c-26120d6ce073"], "manufacturer_name": ["Umasuto, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (85293-005-01)", "package_ndc": "85293-005-01", "marketing_start_date": "20250305"}], "brand_name": "Midodrine Hydrochloride", "product_id": "85293-005_2fb355a4-09cf-880d-e063-6394a90a8178", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "85293-005", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Umasuto, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA207613", "marketing_category": "ANDA", "marketing_start_date": "20250305", "listing_expiration_date": "20261231"}