inzirqo

Generic: hydrochlorothiazide

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name inzirqo
Generic Name hydrochlorothiazide
Labeler ani pharmaceuticals, inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

hydrochlorothiazide 10 mg/mL

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70954-522
Product ID 70954-522_d6ace9b2-f8fa-42b9-8338-9e2b5519ef6b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA219141
Listing Expiration 2026-12-31
Marketing Start 2025-01-30

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 70954522
Hyphenated Format 70954-522

Supplemental Identifiers

RxCUI
2704012 2704018
UPC
0370954522102
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 inzirqo (source: ndc)
Generic Name hydrochlorothiazide (source: ndc)
Application Number NDA219141 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 80 mL in 1 BOTTLE (70954-522-10)
source: ndc

Packages (1)

70954-522-10 80 mL in 1 BOTTLE (70954-522-10)

Ingredients (1)

hydrochlorothiazide (10 mg/mL)

Linked Drug Pages (1)

INZIRQO ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d6ace9b2-f8fa-42b9-8338-9e2b5519ef6b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0370954522102"], "unii": ["0J48LPH2TH"], "rxcui": ["2704012", "2704018"], "spl_set_id": ["41aaea48-6c1b-42c8-a96f-5923d49dc934"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 mL in 1 BOTTLE (70954-522-10)", "package_ndc": "70954-522-10", "marketing_start_date": "20250130"}], "brand_name": "INZIRQO", "product_id": "70954-522_d6ace9b2-f8fa-42b9-8338-9e2b5519ef6b", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70954-522", "generic_name": "hydrochlorothiazide", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "INZIRQO", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "10 mg/mL"}], "application_number": "NDA219141", "marketing_category": "NDA", "marketing_start_date": "20250130", "listing_expiration_date": "20261231"}