Package 60687-409-25

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-409-25
Digits Only 6068740925
Product NDC 60687-409
Description

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

Marketing

Marketing Status
Marketed Since 2018-09-07
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": "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"}