sodium chloride (63323-623)

Drug Facts

Product Profile

Brand Name sodium chloride

Generic Name sodium chloride

Labeler fresenius kabi usa, llc

Dosage Form INJECTION, SOLUTION

Routes

INTRAVENOUS

Active Ingredients

sodium chloride 9 mg/mL

Manufacturer

Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-623

Product ID 63323-623_b9f9ae0e-b72d-480a-b1cc-41d817aa83be

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA207310

Listing Expiration 2026-12-31

Marketing Start 2017-09-19

Pharmacologic Class

Classes

increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63323623

Hyphenated Format 63323-623

Supplemental Identifiers

RxCUI

1807631 1807632 1807633 1807634 1807639

UNII

451W47IQ8X

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 sodium chloride (source: ndc)

Generic Name sodium chloride (source: ndc)

Application Number ANDA207310 (source: ndc)

Routes

INTRAVENOUS

source: ndc

Resolved Composition

Strengths

9 mg/mL

source: ndc

Packaging

50 mL in 1 BAG (63323-623-53)
100 mL in 1 BAG (63323-623-61)
250 mL in 1 BAG (63323-623-74)
500 mL in 1 BAG (63323-623-75)
1000 mL in 1 BAG (63323-623-76)

source: ndc

Packages (5)

63323-623-53 50 mL in 1 BAG (63323-623-53) 63323-623-61 100 mL in 1 BAG (63323-623-61) 63323-623-74 250 mL in 1 BAG (63323-623-74) 63323-623-75 500 mL in 1 BAG (63323-623-75) 63323-623-76 1000 mL in 1 BAG (63323-623-76)

Ingredients (1)

sodium chloride (9 mg/mL)

Linked Drug Pages (1)

Sodium chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAVENOUS"], "spl_id": "b9f9ae0e-b72d-480a-b1cc-41d817aa83be", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807631", "1807632", "1807633", "1807634", "1807639"], "spl_set_id": ["c1e52670-c85e-4f19-a2e9-bf9abd7c3727"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BAG (63323-623-53)", "package_ndc": "63323-623-53", "marketing_start_date": "20170919"}, {"sample": false, "description": "100 mL in 1 BAG (63323-623-61)", "package_ndc": "63323-623-61", "marketing_start_date": "20170919"}, {"sample": false, "description": "250 mL in 1 BAG (63323-623-74)", "package_ndc": "63323-623-74", "marketing_start_date": "20170919"}, {"sample": false, "description": "500 mL in 1 BAG (63323-623-75)", "package_ndc": "63323-623-75", "marketing_start_date": "20170919"}, {"sample": false, "description": "1000 mL in 1 BAG (63323-623-76)", "package_ndc": "63323-623-76", "marketing_start_date": "20170919"}], "brand_name": "Sodium chloride", "product_id": "63323-623_b9f9ae0e-b72d-480a-b1cc-41d817aa83be", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "63323-623", "generic_name": "SODIUM CHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "ANDA207310", "marketing_category": "ANDA", "marketing_start_date": "20170919", "listing_expiration_date": "20261231"}