hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 50 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-449
Product ID 62135-449_459c0f0e-ee69-96b0-e063-6294a90a03a1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085182
Listing Expiration 2026-12-31
Marketing Start 2015-01-15

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 62135449
Hyphenated Format 62135-449

Supplemental Identifiers

RxCUI
197770 310798 429503
UPC
0362135449902 0362135448059 0362135448905 0362135738907 0362135449056
UNII
0J48LPH2TH
NUI
N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager
true

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 ANDA085182 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (62135-449-05)
  • 90 TABLET in 1 BOTTLE (62135-449-90)
source: ndc

Packages (2)

62135-449-05 500 TABLET in 1 BOTTLE (62135-449-05) 62135-449-90 90 TABLET in 1 BOTTLE (62135-449-90)

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": "459c0f0e-ee69-96b0-e063-6294a90a03a1", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0362135449902", "0362135448059", "0362135448905", "0362135738907", "0362135449056"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["4e43dd27-3f4b-4205-a26e-6ecaa8281347"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (62135-449-05)", "package_ndc": "62135-449-05", "marketing_start_date": "20230119"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-449-90)", "package_ndc": "62135-449-90", "marketing_start_date": "20230119"}], "brand_name": "Hydrochlorothiazide", "product_id": "62135-449_459c0f0e-ee69-96b0-e063-6294a90a03a1", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "62135-449", "generic_name": "Hydrochlorothiazide", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA085182", "marketing_category": "ANDA", "marketing_start_date": "20150115", "listing_expiration_date": "20261231"}