Diluent

Generic: water

Labeler: GlaxoSmithKline LLC
NDC Directory HUMAN PRESCRIPTION DRUG NDA Active

Drug Facts

Product Profile

Brand Name Diluent
Generic Name water
Labeler GlaxoSmithKline LLC
Dosage Form SOLUTION
Routes
INTRAVENOUS
Active Ingredients

WATER 1 mL/mL

Identifiers & Regulatory

Product NDC 0173-0857
Product ID 0173-0857_5e54002e-7b03-46ad-ae01-c76c76967201
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020444
Listing Expiration 2026-12-31
Marketing Start 2016-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01730857
Hyphenated Format 0173-0857

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 Diluent (source: ndc)
Generic Name water (source: ndc)
Application Number NDA020444 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 2 VIAL in 1 TRAY (0173-0857-02) / 50 mL in 1 VIAL
source: ndc

Packages (1)

0173-0857-02 2 VIAL in 1 TRAY (0173-0857-02) / 50 mL in 1 VIAL

Ingredients (1)

WATER (1 mL/mL)

Linked Drug Pages (1)

FLOLAN, Diluent ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "5e54002e-7b03-46ad-ae01-c76c76967201", "openfda": {"unii": ["059QF0KO0R", "4K04IQ1OF4"], "rxcui": ["211199", "211200", "562501", "562502"], "spl_set_id": ["8e4b636e-ee9c-4111-779d-28c8369d283b"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL in 1 TRAY (0173-0857-02)  / 50 mL in 1 VIAL", "package_ndc": "0173-0857-02", "marketing_start_date": "20160401"}], "brand_name": "Diluent", "product_id": "0173-0857_5e54002e-7b03-46ad-ae01-c76c76967201", "dosage_form": "SOLUTION", "product_ndc": "0173-0857", "generic_name": "water", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diluent", "active_ingredients": [{"name": "WATER", "strength": "1 mL/mL"}], "application_number": "NDA020444", "marketing_category": "NDA", "marketing_start_date": "20160401", "listing_expiration_date": "20261231"}