Package 70771-1362-5

Brand: triamterene and hydrochlorothiazide

Generic: triamterene and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 70771-1362-5
Digits Only 7077113625
Product NDC 70771-1362
Description

500 TABLET in 1 BOTTLE (70771-1362-5)

Marketing

Marketing Status
Marketed Since 2018-09-04
Brand triamterene and hydrochlorothiazide
Generic triamterene and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b1be913-613c-469c-8665-13858922d5bf", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812", "310818"], "spl_set_id": ["1af80800-e7a5-42e5-aa6c-3f61aff4a77b"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]", "Decreased Renal K+ Excretion [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Potassium-sparing Diuretic [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70771-1362-0)", "package_ndc": "70771-1362-0", "marketing_start_date": "20180904"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1362-1)", "package_ndc": "70771-1362-1", "marketing_start_date": "20180904"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1362-4)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "70771-1362-4", "marketing_start_date": "20180904"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1362-5)", "package_ndc": "70771-1362-5", "marketing_start_date": "20180904"}], "brand_name": "triamterene and hydrochlorothiazide", "product_id": "70771-1362_1b1be913-613c-469c-8665-13858922d5bf", "dosage_form": "TABLET", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70771-1362", "generic_name": "triamterene and hydrochlorothiazide", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "triamterene and hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}, {"name": "TRIAMTERENE", "strength": "75 mg/1"}], "application_number": "ANDA208360", "marketing_category": "ANDA", "marketing_start_date": "20180904", "listing_expiration_date": "20261231"}