Package 52817-324-10

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 52817-324-10
Digits Only 5281732410
Product NDC 52817-324
Description

100 TABLET in 1 BOTTLE (52817-324-10)

Marketing

Marketing Status
Marketed Since 2019-08-19
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": "b8d7c553-3894-7d6d-e053-2a95a90ae868", "openfda": {"upc": ["0352817324108", "0352817323101", "0352817325105"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["a88cd5b5-bdcb-4ef7-8b04-ee4603bcd621"], "manufacturer_name": ["TruPharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (52817-324-10)", "package_ndc": "52817-324-10", "marketing_start_date": "20190819"}], "brand_name": "Midodrine Hydrochloride", "product_id": "52817-324_b8d7c553-3894-7d6d-e053-2a95a90ae868", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "52817-324", "generic_name": "Midodrine Hydrochloride", "labeler_name": "TruPharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA212543", "marketing_category": "ANDA", "marketing_start_date": "20190819", "listing_expiration_date": "20261231"}