midodrine hydrochloride
Generic: midodrine hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
midodrine hydrochloride
Generic Name
midodrine hydrochloride
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
midodrine hydrochloride 2.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-387
Product ID
60687-387_24345c08-4ac2-127f-e063-6294a90aef9a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077746
Listing Expiration
2026-12-31
Marketing Start
2019-06-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687387
Hyphenated Format
60687-387
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
ANDA077746 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-387-01) / 1 TABLET in 1 BLISTER PACK (60687-387-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-387-01) / 1 TABLET in 1 BLISTER PACK (60687-387-11)", "package_ndc": "60687-387-01", "marketing_start_date": "20190605"}], "brand_name": "Midodrine Hydrochloride", "product_id": "60687-387_24345c08-4ac2-127f-e063-6294a90aef9a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "60687-387", "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": "2.5 mg/1"}], "application_number": "ANDA077746", "marketing_category": "ANDA", "marketing_start_date": "20190605", "listing_expiration_date": "20261231"}