Package 68071-3942-3

Brand: metoprolol tartrate

Generic: metoprolol
NDC Package

Package Facts

Identity

Package NDC 68071-3942-3
Digits Only 6807139423
Product NDC 68071-3942
Product ID 68071-3942_47d11563-2d6a-623f-e063-6294a90a54c3
Description

30 TABLET in 1 BOTTLE (68071-3942-3)

Marketing

Marketing Status
Marketed Since 2026-01-07
Brand metoprolol tartrate
Generic metoprolol
Sample Package No

Linked Drug Pages (1)

METOPROLOL TARTRATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47d11563-2d6a-623f-e063-6294a90a54c3", "openfda": {"upc": ["0368071394238"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["47d11c0c-82dd-33b1-e063-6394a90a6a97"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3942-3)", "package_ndc": "68071-3942-3", "marketing_start_date": "20260107"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "68071-3942_47d11563-2d6a-623f-e063-6294a90a54c3", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3942", "generic_name": "METOPROLOL", "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": "ANDA202871", "marketing_category": "ANDA", "marketing_start_date": "20160731", "listing_expiration_date": "20271231"}