Package 68071-4755-9

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 68071-4755-9
Digits Only 6807147559
Product NDC 68071-4755
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-4755-9)

Marketing

Marketing Status
Marketed Since 2019-02-06
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": "1adb4a4f-d32c-c9cb-e063-6394a90a9f51", "openfda": {"upc": ["0368071475531"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["813d0b50-26d6-f732-e053-2991aa0ae24a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68071-4755-2)", "package_ndc": "68071-4755-2", "marketing_start_date": "20190206"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (68071-4755-8)", "package_ndc": "68071-4755-8", "marketing_start_date": "20190206"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-4755-9)", "package_ndc": "68071-4755-9", "marketing_start_date": "20190206"}], "brand_name": "Metoprolol Tartrate", "product_id": "68071-4755_1adb4a4f-d32c-c9cb-e063-6394a90a9f51", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-4755", "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"}