hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: legacy pharmaceutical packaging, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler legacy pharmaceutical packaging, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 25 mg/1

Manufacturer
Legacy Pharmaceutical Packaging, LLC

Identifiers & Regulatory

Product NDC 68645-510
Product ID 68645-510_4c4a2035-8173-6708-e063-6294a90ad6f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA083177
Listing Expiration 2027-12-31
Marketing Start 1973-01-12

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 68645510
Hyphenated Format 68645-510

Supplemental Identifiers

RxCUI
310798
UPC
0368645510545
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 ANDA083177 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68645-510-54)
source: ndc

Packages (1)

68645-510-54 30 TABLET in 1 BOTTLE (68645-510-54)

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": "4c4a2035-8173-6708-e063-6294a90ad6f2", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368645510545"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["1d6ea4b4-1e3c-4f3f-989c-1a3a3c0da6bd"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68645-510-54)", "package_ndc": "68645-510-54", "marketing_start_date": "19730112"}], "brand_name": "Hydrochlorothiazide", "product_id": "68645-510_4c4a2035-8173-6708-e063-6294a90ad6f2", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68645-510", "generic_name": "Hydrochlorothiazide", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA083177", "marketing_category": "ANDA", "marketing_start_date": "19730112", "listing_expiration_date": "20271231"}