Package 68071-3946-3

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 68071-3946-3
Digits Only 6807139463
Product NDC 68071-3946
Description

30 TABLET in 1 BOTTLE (68071-3946-3)

Marketing

Marketing Status
Marketed Since 2026-01-14
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": "485ccc60-7d5e-a87b-e063-6394a90a47dc", "openfda": {"upc": ["0368071394634"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["485f1fdb-6543-4f47-e063-6394a90a2459"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3946-3)", "package_ndc": "68071-3946-3", "marketing_start_date": "20260114"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "68071-3946_485ccc60-7d5e-a87b-e063-6394a90a47dc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3946", "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": "50 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20240117", "listing_expiration_date": "20271231"}