midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler avkare
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 2.5 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-560
Product ID 42291-560_485ffcea-c65d-bf10-e063-6294a90a4ee1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077746
Listing Expiration 2027-12-31
Marketing Start 2017-05-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42291560
Hyphenated Format 42291-560

Supplemental Identifiers

RxCUI
993462 993466 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 ANDA077746 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (42291-560-90)
source: ndc

Packages (1)

Ingredients (1)

midodrine hydrochloride (2.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "485ffcea-c65d-bf10-e063-6294a90a4ee1", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["1c2e8707-550f-430f-87f3-4bb3d55f4aba"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-560-90)", "package_ndc": "42291-560-90", "marketing_start_date": "20170505"}], "brand_name": "Midodrine Hydrochloride", "product_id": "42291-560_485ffcea-c65d-bf10-e063-6294a90a4ee1", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "42291-560", "generic_name": "Midodrine Hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA077746", "marketing_category": "ANDA", "marketing_start_date": "20170505", "listing_expiration_date": "20271231"}