midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: mylan institutional inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler mylan institutional inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 5 mg/1

Manufacturer
Mylan Institutional Inc.

Identifiers & Regulatory

Product NDC 51079-453
Product ID 51079-453_3a8743bb-679f-ae20-e063-6394a90a41c6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076577
Listing Expiration 2026-12-31
Marketing Start 2006-09-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51079453
Hyphenated Format 51079-453

Supplemental Identifiers

RxCUI
993470
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 ANDA076577 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (51079-453-20) / 1 TABLET in 1 BLISTER PACK (51079-453-01)
source: ndc

Packages (1)

Ingredients (1)

midodrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a8743bb-679f-ae20-e063-6394a90a41c6", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993470"], "spl_set_id": ["fd28d383-add9-42a9-ad07-4d7e89f12460"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-453-20)  / 1 TABLET in 1 BLISTER PACK (51079-453-01)", "package_ndc": "51079-453-20", "marketing_start_date": "20060911"}], "brand_name": "Midodrine Hydrochloride", "product_id": "51079-453_3a8743bb-679f-ae20-e063-6394a90a41c6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "51079-453", "generic_name": "midodrine hydrochloride", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076577", "marketing_category": "ANDA", "marketing_start_date": "20060911", "listing_expiration_date": "20261231"}