midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: first nation group, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler first nation group, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 5 mg/1

Manufacturer
First Nation Group, LLC

Identifiers & Regulatory

Product NDC 81469-140
Product ID 81469-140_6e30fa38-fd26-4d37-a5f4-9e044c383362
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217271
Listing Expiration 2026-12-31
Marketing Start 2025-08-13

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81469140
Hyphenated Format 81469-140

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 ANDA217271 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (81469-140-90)
source: ndc

Packages (1)

81469-140-90 90 TABLET in 1 BOTTLE (81469-140-90)

Ingredients (1)

midodrine hydrochloride (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": "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 (81469-140-90)", "package_ndc": "81469-140-90", "marketing_start_date": "20250813"}], "brand_name": "Midodrine Hydrochloride", "product_id": "81469-140_6e30fa38-fd26-4d37-a5f4-9e044c383362", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "81469-140", "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": "5 mg/1"}], "application_number": "ANDA217271", "marketing_category": "ANDA", "marketing_start_date": "20250813", "listing_expiration_date": "20261231"}