Package 68462-842-13
Brand: telmisartan and hydrochlorothiazide
Generic: telmisartan and hydrochlorothiazidePackage Facts
Identity
Package NDC
68462-842-13
Digits Only
6846284213
Product NDC
68462-842
Description
3 BLISTER PACK in 1 CARTON (68462-842-13) / 10 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
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": "697f1231-2483-4e0b-9e23-aeb576fa6171", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0368462842133", "0368462841136", "0368462840139"], "unii": ["0J48LPH2TH", "U5SYW473RQ"], "rxcui": ["283316", "283317", "477130"], "spl_set_id": ["1e55800d-f77c-4950-a6d7-2055f4c7ea17"], "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": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68462-842-13) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "68462-842-13", "marketing_start_date": "20190304"}], "brand_name": "Telmisartan and Hydrochlorothiazide", "product_id": "68462-842_697f1231-2483-4e0b-9e23-aeb576fa6171", "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": "68462-842", "generic_name": "Telmisartan and Hydrochlorothiazide", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "TELMISARTAN", "strength": "80 mg/1"}], "application_number": "ANDA202544", "marketing_category": "ANDA", "marketing_start_date": "20190304", "listing_expiration_date": "20271231"}