hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 25 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-593
Product ID 60687-593_437e73ad-d1f0-3abe-e063-6394a90aa09d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040412
Listing Expiration 2026-12-31
Marketing Start 2021-03-12

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 60687593
Hyphenated Format 60687-593

Supplemental Identifiers

RxCUI
310798
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 ANDA040412 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-593-01) / 1 TABLET in 1 BLISTER PACK (60687-593-11)
source: ndc

Packages (1)

60687-593-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-593-01) / 1 TABLET in 1 BLISTER PACK (60687-593-11)

Ingredients (1)

hydrochlorothiazide (25 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": "437e73ad-d1f0-3abe-e063-6394a90aa09d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["c8de63da-b6c0-42f0-9d47-e273fe93adb3"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-593-01)  / 1 TABLET in 1 BLISTER PACK (60687-593-11)", "package_ndc": "60687-593-01", "marketing_start_date": "20210312"}], "brand_name": "Hydrochlorothiazide", "product_id": "60687-593_437e73ad-d1f0-3abe-e063-6394a90aa09d", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "60687-593", "generic_name": "Hydrochlorothiazide", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA040412", "marketing_category": "ANDA", "marketing_start_date": "20210312", "listing_expiration_date": "20261231"}