Package 63739-145-10

Brand: Midodrine Hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63739-145-10
Digits Only 6373914510
Product NDC 63739-145
Description

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

Marketing

Marketing Status
Discontinued 2026-02-28
Brand Midodrine Hydrochloride
Generic midodrine hydrochloride
Sample Package No

Linked Drug Pages (1)

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"}