hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6156
Product ID 50090-6156_18195385-c154-498f-8ff1-3583c5d5d717
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA087068
Listing Expiration 2027-12-31
Marketing Start 2020-09-25

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 500906156
Hyphenated Format 50090-6156

Supplemental Identifiers

RxCUI
197770
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 ANDA087068 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-6156-0)
  • 100 TABLET in 1 BOTTLE (50090-6156-1)
  • 90 TABLET in 1 BOTTLE (50090-6156-8)
source: ndc

Packages (3)

50090-6156-0 30 TABLET in 1 BOTTLE (50090-6156-0) 50090-6156-1 100 TABLET in 1 BOTTLE (50090-6156-1) 50090-6156-8 90 TABLET in 1 BOTTLE (50090-6156-8)

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": "18195385-c154-498f-8ff1-3583c5d5d717", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["0dbc5ebb-99ab-428d-b9b3-cd7a68dd948a"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6156-0)", "package_ndc": "50090-6156-0", "marketing_start_date": "20221006"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6156-1)", "package_ndc": "50090-6156-1", "marketing_start_date": "20221006"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6156-8)", "package_ndc": "50090-6156-8", "marketing_start_date": "20221006"}], "brand_name": "Hydrochlorothiazide", "product_id": "50090-6156_18195385-c154-498f-8ff1-3583c5d5d717", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "50090-6156", "generic_name": "Hydrochlorothiazide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA087068", "marketing_category": "ANDA", "marketing_start_date": "20200925", "listing_expiration_date": "20271231"}