Package 68071-3943-1
Brand: metoprolol succinate
Generic: metoprolol succinatePackage Facts
Identity
Package NDC
68071-3943-1
Digits Only
6807139431
Product NDC
68071-3943
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3943-1)
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": "47f96afd-1484-66d5-e063-6294a90a201f", "openfda": {"upc": ["0368071394313"], "unii": ["W5S57Y3A5L"], "rxcui": ["866436"], "spl_set_id": ["47f96afd-1483-66d5-e063-6294a90a201f"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3943-1)", "package_ndc": "68071-3943-1", "marketing_start_date": "20260109"}], "brand_name": "Metoprolol Succinate", "product_id": "68071-3943_47f96afd-1484-66d5-e063-6294a90a201f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3943", "generic_name": "Metoprolol Succinate", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA207206", "marketing_category": "ANDA", "marketing_start_date": "20220427", "listing_expiration_date": "20271231"}