Package 63629-7468-3
Brand: irbesartan and hydrochlorothiazide
Generic: irbesartan and hydrochlorothiazidePackage Facts
Identity
Package NDC
63629-7468-3
Digits Only
6362974683
Product NDC
63629-7468
Description
28 TABLET, FILM COATED in 1 BOTTLE (63629-7468-3)
Marketing
Marketing Status
Brand
irbesartan and hydrochlorothiazide
Generic
irbesartan and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9f27724f-cd5c-4885-aa5b-70896904d570", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "unii": ["0J48LPH2TH", "J0E2756Z7N"], "rxcui": ["310792"], "spl_set_id": ["46d77ed8-ece2-4f51-b1a4-4a440e2dce2d"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-7468-1)", "package_ndc": "63629-7468-1", "marketing_start_date": "20190212"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-7468-2)", "package_ndc": "63629-7468-2", "marketing_start_date": "20171120"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (63629-7468-3)", "package_ndc": "63629-7468-3", "marketing_start_date": "20220902"}], "brand_name": "Irbesartan and Hydrochlorothiazide", "product_id": "63629-7468_9f27724f-cd5c-4885-aa5b-70896904d570", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "63629-7468", "generic_name": "Irbesartan and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Irbesartan and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "IRBESARTAN", "strength": "150 mg/1"}], "application_number": "ANDA202414", "marketing_category": "ANDA", "marketing_start_date": "20120927", "listing_expiration_date": "20261231"}