midodrine hydrochloride
Generic: midodrine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
midodrine hydrochloride
Generic Name
midodrine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
midodrine hydrochloride 2.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-1973
Product ID
72162-1973_89d34db8-3963-42bf-8f9a-91b0354f951e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207849
Listing Expiration
2026-12-31
Marketing Start
2020-10-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621973
Hyphenated Format
72162-1973
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
ANDA207849 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (72162-1973-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "89d34db8-3963-42bf-8f9a-91b0354f951e", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993466"], "spl_set_id": ["9c1ccd24-3f9c-489c-9fd2-98e69531d5ab"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1973-1)", "package_ndc": "72162-1973-1", "marketing_start_date": "20240207"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72162-1973_89d34db8-3963-42bf-8f9a-91b0354f951e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72162-1973", "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": "2.5 mg/1"}], "application_number": "ANDA207849", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}