Package 68071-4957-1

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 68071-4957-1
Digits Only 6807149571
Product NDC 68071-4957
Product ID 68071-4957_1b2e48f7-c29a-f37f-e063-6394a90a13dc
Description

100 TABLET, FILM COATED in 1 BOTTLE (68071-4957-1)

Marketing

Marketing Status
Marketed Since 2019-07-03
Brand metoprolol tartrate
Generic metoprolol tartrate
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": "1b2e48f7-c29a-f37f-e063-6394a90a13dc", "openfda": {"upc": ["0368071495713"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["8cce6c9a-2457-18cd-e053-2995a90a3af2"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68071-4957-1)", "package_ndc": "68071-4957-1", "marketing_start_date": "20190703"}], "brand_name": "Metoprolol Tartrate", "product_id": "68071-4957_1b2e48f7-c29a-f37f-e063-6394a90a13dc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-4957", "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": "20181201", "listing_expiration_date": "20261231"}