sodium chloride

Generic: sodium chloride

Labeler: b. braun medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler b. braun medical inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium chloride .9 g/100mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-7800
Product ID 0264-7800_9fa9f6b4-63b5-4632-8104-37c3dd1ee8fa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019635
Listing Expiration 2026-12-31
Marketing Start 1988-03-09

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 02647800
Hyphenated Format 0264-7800

Supplemental Identifiers

RxCUI
1807551 1807552 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 NDA019635 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .9 g/100mL
source: ndc
Packaging
  • 12 CONTAINER in 1 CASE (0264-7800-00) / 1000 mL in 1 CONTAINER
  • 24 CONTAINER in 1 CASE (0264-7800-10) / 500 mL in 1 CONTAINER
  • 24 CONTAINER in 1 CASE (0264-7800-20) / 250 mL in 1 CONTAINER
source: ndc

Packages (3)

0264-7800-00 12 CONTAINER in 1 CASE (0264-7800-00) / 1000 mL in 1 CONTAINER 0264-7800-10 24 CONTAINER in 1 CASE (0264-7800-10) / 500 mL in 1 CONTAINER 0264-7800-20 24 CONTAINER in 1 CASE (0264-7800-20) / 250 mL in 1 CONTAINER

Ingredients (1)

sodium chloride (.9 g/100mL)

Linked Drug Pages (2)

Sodium Chloride ndc-match (0.9) Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "9fa9f6b4-63b5-4632-8104-37c3dd1ee8fa", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807551", "1807552", "1807633", "1807634", "1807639"], "spl_set_id": ["7f22c06b-6b4d-4b49-a4b2-d2169f2bd653"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CONTAINER in 1 CASE (0264-7800-00)  / 1000 mL in 1 CONTAINER", "package_ndc": "0264-7800-00", "marketing_start_date": "19880309"}, {"sample": false, "description": "24 CONTAINER in 1 CASE (0264-7800-10)  / 500 mL in 1 CONTAINER", "package_ndc": "0264-7800-10", "marketing_start_date": "19880309"}, {"sample": false, "description": "24 CONTAINER in 1 CASE (0264-7800-20)  / 250 mL in 1 CONTAINER", "package_ndc": "0264-7800-20", "marketing_start_date": "19880309"}], "brand_name": "Sodium Chloride", "product_id": "0264-7800_9fa9f6b4-63b5-4632-8104-37c3dd1ee8fa", "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": "0264-7800", "generic_name": "SODIUM CHLORIDE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": ".9 g/100mL"}], "application_number": "NDA019635", "marketing_category": "NDA", "marketing_start_date": "19880309", "listing_expiration_date": "20261231"}