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 mg/mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-1800
Product ID 0264-1800_7d4ee37f-5016-422c-9f66-e675ae22c46a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017464
Listing Expiration 2026-12-31
Marketing Start 1978-02-08

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 02641800
Hyphenated Format 0264-1800

Supplemental Identifiers

RxCUI
1807630 1807631 1807632
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 NDA017464 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 84 CONTAINER in 1 CASE (0264-1800-31) / 50 mL in 1 CONTAINER
  • 64 CONTAINER in 1 CASE (0264-1800-32) / 100 mL in 1 CONTAINER
  • 116 CONTAINER in 1 CASE (0264-1800-36) / 25 mL in 1 CONTAINER
source: ndc

Packages (3)

0264-1800-31 84 CONTAINER in 1 CASE (0264-1800-31) / 50 mL in 1 CONTAINER 0264-1800-32 64 CONTAINER in 1 CASE (0264-1800-32) / 100 mL in 1 CONTAINER 0264-1800-36 116 CONTAINER in 1 CASE (0264-1800-36) / 25 mL in 1 CONTAINER

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": "7d4ee37f-5016-422c-9f66-e675ae22c46a", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807630", "1807631", "1807632"], "spl_set_id": ["cc14fafd-3dcd-4fc8-bdbd-6f355c375768"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "84 CONTAINER in 1 CASE (0264-1800-31)  / 50 mL in 1 CONTAINER", "package_ndc": "0264-1800-31", "marketing_start_date": "19780208"}, {"sample": false, "description": "64 CONTAINER in 1 CASE (0264-1800-32)  / 100 mL in 1 CONTAINER", "package_ndc": "0264-1800-32", "marketing_start_date": "19780208"}, {"sample": false, "description": "116 CONTAINER in 1 CASE (0264-1800-36)  / 25 mL in 1 CONTAINER", "package_ndc": "0264-1800-36", "marketing_start_date": "19780208"}], "brand_name": "Sodium Chloride", "product_id": "0264-1800_7d4ee37f-5016-422c-9f66-e675ae22c46a", "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": "0264-1800", "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 mg/mL"}], "application_number": "NDA017464", "marketing_category": "NDA", "marketing_start_date": "19780208", "listing_expiration_date": "20261231"}