Package 68071-3828-1
Brand: metoprolol succinate
Generic: metoprolol succinatePackage Facts
Identity
Package NDC
68071-3828-1
Digits Only
6807138281
Product NDC
68071-3828
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3828-1)
Marketing
Marketing Status
Brand
metoprolol succinate
Generic
metoprolol succinate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32340827-2dbb-dfe5-e063-6294a90ab085", "openfda": {"upc": ["0368071382815"], "unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["32341a31-a2db-cf13-e063-6394a90aad89"], "manufacturer_name": ["NuCare Pharmaceutcals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3828-1)", "package_ndc": "68071-3828-1", "marketing_start_date": "20250407"}], "brand_name": "Metoprolol succinate", "product_id": "68071-3828_32340827-2dbb-dfe5-e063-6294a90ab085", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3828", "generic_name": "Metoprolol succinate", "labeler_name": "NuCare Pharmaceutcals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA090617", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}