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 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1705
Product ID 71335-1705_2be17e48-8258-4f29-914b-7f0fe9ace7a1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207613
Listing Expiration 2026-12-31
Marketing Start 2019-04-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351705
Hyphenated Format 71335-1705

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 ANDA207613 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1705-1)
source: ndc

Packages (1)

71335-1705-1 30 TABLET in 1 BOTTLE (71335-1705-1)

Ingredients (1)

midodrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Midodrine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2be17e48-8258-4f29-914b-7f0fe9ace7a1", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993470"], "spl_set_id": ["2be17e48-8258-4f29-914b-7f0fe9ace7a1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1705-1)", "package_ndc": "71335-1705-1", "marketing_start_date": "20200910"}], "brand_name": "Midodrine Hydrochloride", "product_id": "71335-1705_2be17e48-8258-4f29-914b-7f0fe9ace7a1", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "71335-1705", "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": "5 mg/1"}], "application_number": "ANDA207613", "marketing_category": "ANDA", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}