Package 46708-210-30

Brand: telmisartan and hydrochlorothiazide

Generic: telmisartan and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 46708-210-30
Digits Only 4670821030
Product NDC 46708-210
Description

30 TABLET in 1 BOTTLE (46708-210-30)

Marketing

Marketing Status
Marketed Since 2014-03-14
Brand telmisartan and hydrochlorothiazide
Generic telmisartan and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7c37a82a-77c2-4d49-84ee-ee4f70b4ec93", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0346708211301", "0346708209308", "0346708210304"], "unii": ["0J48LPH2TH", "U5SYW473RQ"], "rxcui": ["283316", "283317", "477130"], "spl_set_id": ["5b476740-e3f0-4f68-b07c-cd9eb2fa27ca"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CARTON (46708-210-10)", "package_ndc": "46708-210-10", "marketing_start_date": "20140314"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (46708-210-30)", "package_ndc": "46708-210-30", "marketing_start_date": "20140314"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (46708-210-91)", "package_ndc": "46708-210-91", "marketing_start_date": "20140314"}], "brand_name": "Telmisartan and Hydrochlorothiazide", "product_id": "46708-210_7c37a82a-77c2-4d49-84ee-ee4f70b4ec93", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "46708-210", "generic_name": "Telmisartan and Hydrochlorothiazide", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "TELMISARTAN", "strength": "80 mg/1"}], "application_number": "ANDA203010", "marketing_category": "ANDA", "marketing_start_date": "20140314", "listing_expiration_date": "20261231"}