Package 68071-5211-2

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 68071-5211-2
Digits Only 6807152112
Product NDC 68071-5211
Product ID 68071-5211_1b57747f-6805-839f-e063-6294a90a860f
Description

120 TABLET in 1 BOTTLE (68071-5211-2)

Marketing

Marketing Status
Marketed Since 2020-03-17
Brand hydrochlorothiazide
Generic hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Hydrochlorothiazide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b57747f-6805-839f-e063-6294a90a860f", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368071521122"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["a111cb8f-a100-a05d-e053-2995a90a020c"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (68071-5211-2)", "package_ndc": "68071-5211-2", "marketing_start_date": "20200317"}], "brand_name": "Hydrochlorothiazide", "product_id": "68071-5211_1b57747f-6805-839f-e063-6294a90a860f", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68071-5211", "generic_name": "Hydrochlorothiazide", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA085182", "marketing_category": "ANDA", "marketing_start_date": "20150115", "listing_expiration_date": "20261231"}