chlorothiazide

Generic: chlorothiazide sodium

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorothiazide
Generic Name chlorothiazide sodium
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

chlorothiazide sodium 500 mg/18mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-658
Product ID 63323-658_85e1af90-9f5e-44a1-8bc3-5868be35812b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090896
Listing Expiration 2026-12-31
Marketing Start 2009-10-21

Pharmacologic Class

Classes
increased diuresis [pe] thiazide diuretic [epc] thiazides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63323658
Hyphenated Format 63323-658

Supplemental Identifiers

RxCUI
484152
UPC
0363323658274
UNII
SN86FG7N2K

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 chlorothiazide (source: ndc)
Generic Name chlorothiazide sodium (source: ndc)
Application Number ANDA090896 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/18mL
source: ndc
Packaging
  • 1 VIAL in 1 BOX (63323-658-27) / 18 mL in 1 VIAL
source: ndc

Packages (1)

63323-658-27 1 VIAL in 1 BOX (63323-658-27) / 18 mL in 1 VIAL

Ingredients (1)

chlorothiazide sodium (500 mg/18mL)

Linked Drug Pages (3)

Chlorothiazide ndc-match (0.9) Chlorothiazide ndc-match (0.9) Chlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "85e1af90-9f5e-44a1-8bc3-5868be35812b", "openfda": {"upc": ["0363323658274"], "unii": ["SN86FG7N2K"], "rxcui": ["484152"], "spl_set_id": ["de250776-461a-4d02-a82e-ffedca1a9cf4"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (63323-658-27)  / 18 mL in 1 VIAL", "package_ndc": "63323-658-27", "marketing_start_date": "20091021"}], "brand_name": "Chlorothiazide", "product_id": "63323-658_85e1af90-9f5e-44a1-8bc3-5868be35812b", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "63323-658", "generic_name": "CHLOROTHIAZIDE SODIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorothiazide", "active_ingredients": [{"name": "CHLOROTHIAZIDE SODIUM", "strength": "500 mg/18mL"}], "application_number": "ANDA090896", "marketing_category": "ANDA", "marketing_start_date": "20091021", "listing_expiration_date": "20261231"}