Package 68071-4687-3
Brand: triamterene and hydrochlorothiazide
Generic: triamterene and hydrochlorothiazidePackage Facts
Identity
Package NDC
68071-4687-3
Digits Only
6807146873
Product NDC
68071-4687
Description
30 TABLET in 1 BOTTLE (68071-4687-3)
Marketing
Marketing Status
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": "1ab8dd17-7094-a50c-e063-6394a90ac292", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "upc": ["0368071468731"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310818"], "spl_set_id": ["7e7cb50d-c984-5c01-e053-2a91aa0a68a5"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4687-3)", "package_ndc": "68071-4687-3", "marketing_start_date": "20190102"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "68071-4687_1ab8dd17-7094-a50c-e063-6394a90ac292", "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": "68071-4687", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "ANDA071851", "marketing_category": "ANDA", "marketing_start_date": "19930923", "listing_expiration_date": "20261231"}