hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 50 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3323
Product ID 68071-3323_1cd709d4-ae48-e5f8-e063-6294a90a07ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202556
Listing Expiration 2026-12-31
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 680713323
Hyphenated Format 68071-3323

Supplemental Identifiers

RxCUI
197770
UPC
0368071332339
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 ANDA202556 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-3323-3)
  • 15 TABLET in 1 BOTTLE (68071-3323-5)
  • 60 TABLET in 1 BOTTLE (68071-3323-6)
  • 90 TABLET in 1 BOTTLE (68071-3323-9)
source: ndc

Packages (4)

68071-3323-3 30 TABLET in 1 BOTTLE (68071-3323-3) 68071-3323-5 15 TABLET in 1 BOTTLE (68071-3323-5) 68071-3323-6 60 TABLET in 1 BOTTLE (68071-3323-6) 68071-3323-9 90 TABLET in 1 BOTTLE (68071-3323-9)

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": "1cd709d4-ae48-e5f8-e063-6294a90a07ee", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368071332339"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["53fe1730-a803-26b2-e054-00144ff88e88"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3323-3)", "package_ndc": "68071-3323-3", "marketing_start_date": "20170710"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68071-3323-5)", "package_ndc": "68071-3323-5", "marketing_start_date": "20170710"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3323-6)", "package_ndc": "68071-3323-6", "marketing_start_date": "20170710"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3323-9)", "package_ndc": "68071-3323-9", "marketing_start_date": "20170710"}], "brand_name": "Hydrochlorothiazide", "product_id": "68071-3323_1cd709d4-ae48-e5f8-e063-6294a90a07ee", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68071-3323", "generic_name": "Hydrochlorothiazide", "labeler_name": "NuCare Pharmaceuticals, 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": "20261231"}