Package 62756-370-88

Brand: metoprolol tartrate and hydrochlorothiazide

Generic: metoprolol tartrate and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 62756-370-88
Digits Only 6275637088
Product NDC 62756-370
Description

100 TABLET in 1 BOTTLE (62756-370-88)

Marketing

Marketing Status
Marketed Since 2022-04-01
Brand metoprolol tartrate and hydrochlorothiazide
Generic metoprolol tartrate and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "99595af6-8c5d-4dc7-8396-e7bce050bb3f", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0362756368880", "0362756369887", "0362756370883"], "unii": ["0J48LPH2TH", "W5S57Y3A5L"], "rxcui": ["866479", "866482", "866491"], "spl_set_id": ["faaf13ce-5d8d-4c57-a49f-a7a73daa41a5"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62756-370-08)", "package_ndc": "62756-370-08", "marketing_start_date": "20220401"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62756-370-18)", "package_ndc": "62756-370-18", "marketing_start_date": "20220401"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62756-370-83)", "package_ndc": "62756-370-83", "marketing_start_date": "20220401"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62756-370-88)", "package_ndc": "62756-370-88", "marketing_start_date": "20220401"}], "brand_name": "Metoprolol Tartrate and Hydrochlorothiazide", "product_id": "62756-370_99595af6-8c5d-4dc7-8396-e7bce050bb3f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62756-370", "generic_name": "Metoprolol Tartrate and Hydrochlorothiazide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA090654", "marketing_category": "ANDA", "marketing_start_date": "20220401", "listing_expiration_date": "20261231"}