dextrose and sodium chloride

Generic: dextrose and sodium chloride

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

Drug Facts

Product Profile

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

dextrose, unspecified form 5 g/100mL, sodium chloride .9 g/100mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-7610
Product ID 0264-7610_1e0af1ae-3754-4327-8037-1eb294c86cb6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019631
Listing Expiration 2026-12-31
Marketing Start 1988-02-24

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 02647610
Hyphenated Format 0264-7610

Supplemental Identifiers

RxCUI
244098 245220 687196 1794881 1794886 1794887 1795170 1795171 1795250 1795252 1795254 1795344 1795346 1795470
UNII
451W47IQ8X IY9XDZ35W2

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 dextrose and sodium chloride (source: ndc)
Generic Name dextrose and sodium chloride (source: ndc)
Application Number NDA019631 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • .9 g/100mL
source: ndc
Packaging
  • 12 CONTAINER in 1 CASE (0264-7610-00) / 1000 mL in 1 CONTAINER
  • 24 CONTAINER in 1 CASE (0264-7610-10) / 500 mL in 1 CONTAINER
source: ndc

Packages (2)

0264-7610-00 12 CONTAINER in 1 CASE (0264-7610-00) / 1000 mL in 1 CONTAINER 0264-7610-10 24 CONTAINER in 1 CASE (0264-7610-10) / 500 mL in 1 CONTAINER

Ingredients (2)

dextrose, unspecified form (5 g/100mL) sodium chloride (.9 g/100mL)

Linked Drug Pages (1)

Dextrose And Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "1e0af1ae-3754-4327-8037-1eb294c86cb6", "openfda": {"unii": ["451W47IQ8X", "IY9XDZ35W2"], "rxcui": ["244098", "245220", "687196", "1794881", "1794886", "1794887", "1795170", "1795171", "1795250", "1795252", "1795254", "1795344", "1795346", "1795470"], "spl_set_id": ["8e6569ce-9714-497f-a94b-c6975c1d76f6"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CONTAINER in 1 CASE (0264-7610-00)  / 1000 mL in 1 CONTAINER", "package_ndc": "0264-7610-00", "marketing_start_date": "19880224"}, {"sample": false, "description": "24 CONTAINER in 1 CASE (0264-7610-10)  / 500 mL in 1 CONTAINER", "package_ndc": "0264-7610-10", "marketing_start_date": "19880224"}], "brand_name": "Dextrose And Sodium Chloride", "product_id": "0264-7610_1e0af1ae-3754-4327-8037-1eb294c86cb6", "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": "0264-7610", "generic_name": "DEXTROSE and SODIUM CHLORIDE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose And Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE, UNSPECIFIED FORM", "strength": "5 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".9 g/100mL"}], "application_number": "NDA019631", "marketing_category": "NDA", "marketing_start_date": "19880224", "listing_expiration_date": "20261231"}