Package 62332-338-71

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62332-338-71
Digits Only 6233233871
Product NDC 62332-338
Description

500 TABLET in 1 BOTTLE (62332-338-71)

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": "f954a150-26a9-4b64-8e86-5d5bc4eedc43", "openfda": {"upc": ["0362332339310", "0362332338313", "0362332340316"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["873c8e29-6961-4648-bfc8-f91c2086bd94"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62332-338-31)", "package_ndc": "62332-338-31", "marketing_start_date": "20210122"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62332-338-71)", "package_ndc": "62332-338-71", "marketing_start_date": "20210122"}], "brand_name": "MIDODRINE HYDROCHLORIDE", "product_id": "62332-338_f954a150-26a9-4b64-8e86-5d5bc4eedc43", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "62332-338", "generic_name": "MIDODRINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MIDODRINE HYDROCHLORIDE", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA214734", "marketing_category": "ANDA", "marketing_start_date": "20210122", "listing_expiration_date": "20261231"}