diuril

Generic: chlorothiazide

Labeler: salix pharmaceuticals, inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name diuril
Generic Name chlorothiazide
Labeler salix pharmaceuticals, inc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

chlorothiazide 250 mg/5mL

Manufacturer
Salix Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 65649-311
Product ID 65649-311_7875229f-e08f-4443-9980-d2ca6fab68f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA011870
Listing Expiration 2026-12-31
Marketing Start 1962-02-15

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 65649311
Hyphenated Format 65649-311

Supplemental Identifiers

RxCUI
213439 309198
UNII
77W477J15H
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 diuril (source: ndc)
Generic Name chlorothiazide (source: ndc)
Application Number NDA011870 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (65649-311-12) / 237 mL in 1 BOTTLE
source: ndc

Packages (1)

65649-311-12 1 BOTTLE in 1 CARTON (65649-311-12) / 237 mL in 1 BOTTLE

Ingredients (1)

chlorothiazide (250 mg/5mL)

Linked Drug Pages (1)

DIURIL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7875229f-e08f-4443-9980-d2ca6fab68f7", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["77W477J15H"], "rxcui": ["213439", "309198"], "spl_set_id": ["bd936e35-1af8-42da-bcc0-f22489d68574"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Salix Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (65649-311-12)  / 237 mL in 1 BOTTLE", "package_ndc": "65649-311-12", "marketing_start_date": "19620215"}], "brand_name": "DIURIL", "product_id": "65649-311_7875229f-e08f-4443-9980-d2ca6fab68f7", "dosage_form": "SUSPENSION", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "65649-311", "generic_name": "CHLOROTHIAZIDE", "labeler_name": "Salix Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIURIL", "active_ingredients": [{"name": "CHLOROTHIAZIDE", "strength": "250 mg/5mL"}], "application_number": "NDA011870", "marketing_category": "NDA", "marketing_start_date": "19620215", "listing_expiration_date": "20261231"}