Package 68071-3941-6
Brand: metoprolol tartrate
Generic: metoprolol tartratePackage Facts
Identity
Package NDC
68071-3941-6
Digits Only
6807139416
Product NDC
68071-3941
Description
60 TABLET, FILM COATED in 1 BOTTLE (68071-3941-6)
Marketing
Marketing Status
Brand
metoprolol tartrate
Generic
metoprolol tartrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47d18ba7-558c-1190-e063-6294a90a958f", "openfda": {"upc": ["0368071394160"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["47d18ba7-558d-1190-e063-6294a90a958f"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-3941-6)", "package_ndc": "68071-3941-6", "marketing_start_date": "20260107"}], "brand_name": "Metoprolol Tartrate", "product_id": "68071-3941_47d18ba7-558c-1190-e063-6294a90a958f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3941", "generic_name": "Metoprolol Tartrate", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20271231"}