Package 71205-063-30

Brand: irbesartan and hydrochlorothiazide

Generic: irbesartan and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 71205-063-30
Digits Only 7120506330
Product NDC 71205-063
Description

30 TABLET in 1 BOTTLE (71205-063-30)

Marketing

Marketing Status
Marketed Since 2018-07-02
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": "7e2cab03-6f27-497c-a574-b99f9d4d7317", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "unii": ["0J48LPH2TH", "J0E2756Z7N"], "rxcui": ["310792"], "spl_set_id": ["c7ce5a69-1e07-4d52-b815-ce64ac3731ac"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-063-30)", "package_ndc": "71205-063-30", "marketing_start_date": "20180702"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-063-60)", "package_ndc": "71205-063-60", "marketing_start_date": "20180702"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-063-90)", "package_ndc": "71205-063-90", "marketing_start_date": "20180702"}], "brand_name": "Irbesartan and Hydrochlorothiazide", "product_id": "71205-063_7e2cab03-6f27-497c-a574-b99f9d4d7317", "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": "71205-063", "generic_name": "Irbesartan and Hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "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": "ANDA203072", "marketing_category": "ANDA", "marketing_start_date": "20140301", "listing_expiration_date": "20261231"}