hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: accord healthcare inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler accord healthcare inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 50 mg/1

Manufacturer
Accord Healthcare Inc.

Identifiers & Regulatory

Product NDC 16729-184
Product ID 16729-184_4b95022b-87b4-60ac-e063-6294a90afa9b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202556
Listing Expiration 2027-12-31
Marketing Start 2013-04-10

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 16729184
Hyphenated Format 16729-184

Supplemental Identifiers

RxCUI
197770 310798 429503
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 ANDA202556 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (16729-184-01)
  • 1000 TABLET in 1 BOTTLE (16729-184-17)
source: ndc

Packages (2)

16729-184-01 100 TABLET in 1 BOTTLE (16729-184-01) 16729-184-17 1000 TABLET in 1 BOTTLE (16729-184-17)

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": "4b95022b-87b4-60ac-e063-6294a90afa9b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["babb1b20-fe82-40ba-8e7a-0c56fe433b4a"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16729-184-01)", "package_ndc": "16729-184-01", "marketing_start_date": "20130426"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16729-184-17)", "package_ndc": "16729-184-17", "marketing_start_date": "20130410"}], "brand_name": "Hydrochlorothiazide", "product_id": "16729-184_4b95022b-87b4-60ac-e063-6294a90afa9b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "16729-184", "generic_name": "Hydrochlorothiazide", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA202556", "marketing_category": "ANDA", "marketing_start_date": "20130410", "listing_expiration_date": "20271231"}