midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 10 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-409
Product ID 60687-409_24345c08-4ac2-127f-e063-6294a90aef9a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077746
Listing Expiration 2026-12-31
Marketing Start 2018-09-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687409
Hyphenated Format 60687-409

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
  • 10 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-409-25) / 1 TABLET in 1 BLISTER PACK (60687-409-95)
source: ndc

Packages (1)

60687-409-25 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-409-25) / 1 TABLET in 1 BLISTER PACK (60687-409-95)

Ingredients (1)

midodrine hydrochloride (10 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": "24345c08-4ac2-127f-e063-6294a90aef9a", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["159cb0cb-4b27-4a1c-8ad4-dc93604c79c7"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-409-25)  / 1 TABLET in 1 BLISTER PACK (60687-409-95)", "package_ndc": "60687-409-25", "marketing_start_date": "20180907"}], "brand_name": "Midodrine Hydrochloride", "product_id": "60687-409_24345c08-4ac2-127f-e063-6294a90aef9a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "60687-409", "generic_name": "Midodrine Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077746", "marketing_category": "ANDA", "marketing_start_date": "20180907", "listing_expiration_date": "20261231"}