midodrine hydrochloride
Generic: midodrine hydrochloride
Labeler: mylan institutional inc.Drug Facts
Product Profile
Brand Name
midodrine hydrochloride
Generic Name
midodrine hydrochloride
Labeler
mylan institutional inc.
Dosage Form
TABLET
Routes
Active Ingredients
midodrine hydrochloride 5 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51079453
Hyphenated Format
51079-453
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (51079-453-20) / 1 TABLET in 1 BLISTER PACK (51079-453-01)
Packages (1)
Ingredients (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"}