hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-9647
Product ID 71335-9647_45686a7b-3601-4db4-b7cd-866de3c21f40
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040702
Listing Expiration 2026-12-31
Marketing Start 2019-11-01

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 713359647
Hyphenated Format 71335-9647

Supplemental Identifiers

RxCUI
429503
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 ANDA040702 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (71335-9647-1)
  • 90 TABLET in 1 BOTTLE, PLASTIC (71335-9647-2)
  • 14 TABLET in 1 BOTTLE, PLASTIC (71335-9647-3)
  • 100 TABLET in 1 BOTTLE, PLASTIC (71335-9647-4)
source: ndc

Packages (4)

71335-9647-1 30 TABLET in 1 BOTTLE, PLASTIC (71335-9647-1) 71335-9647-2 90 TABLET in 1 BOTTLE, PLASTIC (71335-9647-2) 71335-9647-3 14 TABLET in 1 BOTTLE, PLASTIC (71335-9647-3) 71335-9647-4 100 TABLET in 1 BOTTLE, PLASTIC (71335-9647-4)

Ingredients (1)

hydrochlorothiazide (12.5 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": "45686a7b-3601-4db4-b7cd-866de3c21f40", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["03b7e52e-0003-47c3-af12-93ef00800b37"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71335-9647-1)", "package_ndc": "71335-9647-1", "marketing_start_date": "20240220"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71335-9647-2)", "package_ndc": "71335-9647-2", "marketing_start_date": "20230720"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (71335-9647-3)", "package_ndc": "71335-9647-3", "marketing_start_date": "20240906"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (71335-9647-4)", "package_ndc": "71335-9647-4", "marketing_start_date": "20240906"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "71335-9647_45686a7b-3601-4db4-b7cd-866de3c21f40", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71335-9647", "generic_name": "HYDROCHLOROTHIAZIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040702", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}