hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-751
Product ID 71205-751_c4fe84e3-c291-4220-95c1-a2bd02b1e134
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA083177
Listing Expiration 2026-12-31
Marketing Start 1980-01-07

Pharmacologic Class

Established (EPC)
thiazide diuretic [epc]
Chemical Structure
thiazides [cs]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205751
Hyphenated Format 71205-751

Supplemental Identifiers

RxCUI
197770
UPC
0371205751906
UNII
0J48LPH2TH
NUI
N0000175359 N0000175419 M0471776

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name hydrochlorothiazide (source: ndc)
Generic Name hydrochlorothiazide (source: ndc)
Application Number ANDA083177 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-751-30)
  • 60 TABLET in 1 BOTTLE (71205-751-60)
  • 90 TABLET in 1 BOTTLE (71205-751-90)
source: ndc

Packages (3)

71205-751-30 30 TABLET in 1 BOTTLE (71205-751-30) 71205-751-60 60 TABLET in 1 BOTTLE (71205-751-60) 71205-751-90 90 TABLET in 1 BOTTLE (71205-751-90)

Ingredients (1)

hydrochlorothiazide (50 mg/1)

Linked Drug Pages (1)

Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c4fe84e3-c291-4220-95c1-a2bd02b1e134", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0371205751906"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["c4fe84e3-c291-4220-95c1-a2bd02b1e134"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-751-30)", "package_ndc": "71205-751-30", "marketing_start_date": "20230202"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-751-60)", "package_ndc": "71205-751-60", "marketing_start_date": "20230202"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-751-90)", "package_ndc": "71205-751-90", "marketing_start_date": "20230202"}], "brand_name": "Hydrochlorothiazide", "product_id": "71205-751_c4fe84e3-c291-4220-95c1-a2bd02b1e134", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71205-751", "generic_name": "Hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA083177", "marketing_category": "ANDA", "marketing_start_date": "19800107", "listing_expiration_date": "20261231"}