Package 33342-287-07
Brand: amlodipine,valsartan and hydrochlorothiazide
Generic: amlodipine,valsartan and hydrochlorothiazidePackage Facts
Identity
Package NDC
33342-287-07
Digits Only
3334228707
Product NDC
33342-287
Description
30 TABLET, FILM COATED in 1 BOTTLE (33342-287-07)
Marketing
Marketing Status
Brand
amlodipine,valsartan and hydrochlorothiazide
Generic
amlodipine,valsartan and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ea4f227-b97a-49f1-bbc3-1dede2c1866d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0333342283078", "0333342287076", "0333342284075"], "unii": ["0J48LPH2TH", "864V2Q084H", "80M03YXJ7I"], "rxcui": ["848131", "848135", "848140", "848145", "848151"], "spl_set_id": ["1ea4f227-b97a-49f1-bbc3-1dede2c1866d"], "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": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (33342-287-07)", "package_ndc": "33342-287-07", "marketing_start_date": "20250106"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-287-10)", "package_ndc": "33342-287-10", "marketing_start_date": "20250106"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-287-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "33342-287-12", "marketing_start_date": "20250106"}], "brand_name": "amlodipine,valsartan and hydrochlorothiazide", "product_id": "33342-287_1ea4f227-b97a-49f1-bbc3-1dede2c1866d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "33342-287", "generic_name": "amlodipine,valsartan and hydrochlorothiazide", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "amlodipine,valsartan and hydrochlorothiazide", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA207299", "marketing_category": "ANDA", "marketing_start_date": "20250106", "listing_expiration_date": "20261231"}