hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler rising pharma holdings, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 57237-002
Product ID 57237-002_adc31708-42a5-4529-ab66-b0445d1ba5e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078164
Listing Expiration 2026-12-31
Marketing Start 2007-09-19

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 57237002
Hyphenated Format 57237-002

Supplemental Identifiers

RxCUI
199903
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 ANDA078164 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (57237-002-01)
  • 500 CAPSULE in 1 BOTTLE (57237-002-05)
  • 1000 CAPSULE in 1 BOTTLE (57237-002-99)
source: ndc

Packages (3)

57237-002-01 100 CAPSULE in 1 BOTTLE (57237-002-01) 57237-002-05 500 CAPSULE in 1 BOTTLE (57237-002-05) 57237-002-99 1000 CAPSULE in 1 BOTTLE (57237-002-99)

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": "adc31708-42a5-4529-ab66-b0445d1ba5e8", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["199903"], "spl_set_id": ["33f9c3ae-108d-469e-af6c-8be3b0f83139"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (57237-002-01)", "package_ndc": "57237-002-01", "marketing_start_date": "20070919"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (57237-002-05)", "package_ndc": "57237-002-05", "marketing_start_date": "20070919"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (57237-002-99)", "package_ndc": "57237-002-99", "marketing_start_date": "20070919"}], "brand_name": "Hydrochlorothiazide", "product_id": "57237-002_adc31708-42a5-4529-ab66-b0445d1ba5e8", "dosage_form": "CAPSULE", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "57237-002", "generic_name": "Hydrochlorothiazide", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA078164", "marketing_category": "ANDA", "marketing_start_date": "20070919", "listing_expiration_date": "20261231"}