Package 68382-567-01

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 68382-567-01
Digits Only 6838256701
Product NDC 68382-567
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-567-01)

Marketing

Marketing Status
Marketed Since 2018-06-07
Brand metoprolol succinate
Generic metoprolol succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d89802b-2784-4eeb-977c-299ab20fd53e", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["bd77ec6e-c58c-440b-81d6-8a462b2fdc9c"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-567-01)", "package_ndc": "68382-567-01", "marketing_start_date": "20180607"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-567-05)", "package_ndc": "68382-567-05", "marketing_start_date": "20180607"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-567-10)", "package_ndc": "68382-567-10", "marketing_start_date": "20180607"}], "brand_name": "metoprolol succinate", "product_id": "68382-567_0d89802b-2784-4eeb-977c-299ab20fd53e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68382-567", "generic_name": "metoprolol succinate", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "200 mg/1"}], "application_number": "ANDA203894", "marketing_category": "ANDA", "marketing_start_date": "20180607", "listing_expiration_date": "20261231"}