Package 46708-340-31

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 46708-340-31
Digits Only 4670834031
Product NDC 46708-340
Description

100 TABLET in 1 BOTTLE (46708-340-31)

Marketing

Marketing Status
Marketed Since 2021-01-22
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": "38173ca4-7b7e-4c91-b12c-7cce5bfaba84", "openfda": {"upc": ["0346708339319", "0346708340315", "0346708338312"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["03b54024-2a26-4abe-bd8b-b66bb6781fa7"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (46708-340-31)", "package_ndc": "46708-340-31", "marketing_start_date": "20210122"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (46708-340-71)", "package_ndc": "46708-340-71", "marketing_start_date": "20210122"}], "brand_name": "MIDODRINE HYDROCHLORIDE", "product_id": "46708-340_38173ca4-7b7e-4c91-b12c-7cce5bfaba84", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "46708-340", "generic_name": "MIDODRINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MIDODRINE HYDROCHLORIDE", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214734", "marketing_category": "ANDA", "marketing_start_date": "20210122", "listing_expiration_date": "20261231"}