midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1975
Product ID 72162-1975_58ddb037-7341-4afa-b355-36bc5f8adfd8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207849
Listing Expiration 2026-12-31
Marketing Start 2020-10-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621975
Hyphenated Format 72162-1975

Supplemental Identifiers

RxCUI
993462
UNII
59JV96YTXV

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 ANDA207849 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72162-1975-1)
source: ndc

Packages (1)

Ingredients (1)

midodrine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "58ddb037-7341-4afa-b355-36bc5f8adfd8", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462"], "spl_set_id": ["78446de1-81f6-4764-98f3-44b4057f2175"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1975-1)", "package_ndc": "72162-1975-1", "marketing_start_date": "20240207"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72162-1975_58ddb037-7341-4afa-b355-36bc5f8adfd8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72162-1975", "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": "10 mg/1"}], "application_number": "ANDA207849", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}