Midodrine Hydrochloride

Generic: midodrine hydrochloride

Labeler: McKesson Corporation DBA SKY Packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Midodrine Hydrochloride
Generic Name midodrine hydrochloride
Labeler McKesson Corporation DBA SKY Packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

MIDODRINE HYDROCHLORIDE 5 mg/1

Identifiers & Regulatory

Product NDC 63739-145
Product ID 63739-145_2b39e6ff-aff0-1eba-e063-6394a90a2201
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207849
Marketing Start 2020-10-15
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63739145
Hyphenated Format 63739-145

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-145-10) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

63739-145-10 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-145-10) / 10 TABLET in 1 BLISTER PACK

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": "2b39e6ff-aff0-1eba-e063-6394a90a2201", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993470"], "spl_set_id": ["e81e4324-8264-9ee6-e053-2995a90a8673"], "manufacturer_name": ["McKesson Corporation DBA SKY Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-145-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "63739-145-10", "marketing_end_date": "20260228", "marketing_start_date": "20220908"}], "brand_name": "Midodrine Hydrochloride", "product_id": "63739-145_2b39e6ff-aff0-1eba-e063-6394a90a2201", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "63739-145", "generic_name": "midodrine hydrochloride", "labeler_name": "McKesson Corporation DBA SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA207849", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20201015"}