potassium chloride in dextrose and sodium chloride

Generic: dextrose, sodium chloride, and potassium chloride

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

Drug Facts

Product Profile

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

dextrose, unspecified form 5 g/100mL, potassium chloride .22 g/100mL, sodium chloride .45 g/100mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-7636
Product ID 0264-7636_ed62bbc9-60b1-41c1-ae42-846cb79daa11
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019630
Listing Expiration 2026-12-31
Marketing Start 1988-02-17

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02647636
Hyphenated Format 0264-7636

Supplemental Identifiers

RxCUI
615099 615100 615107 630796 1863605 1863973 1863988 1866190
UNII
660YQ98I10 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 potassium chloride in dextrose and sodium chloride (source: ndc)
Generic Name dextrose, sodium chloride, and potassium chloride (source: ndc)
Application Number NDA019630 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • .22 g/100mL
  • .45 g/100mL
source: ndc
Packaging
  • 12 CONTAINER in 1 CASE (0264-7636-00) / 1000 mL in 1 CONTAINER
source: ndc

Packages (1)

0264-7636-00 12 CONTAINER in 1 CASE (0264-7636-00) / 1000 mL in 1 CONTAINER

Ingredients (3)

dextrose, unspecified form (5 g/100mL) potassium chloride (.22 g/100mL) sodium chloride (.45 g/100mL)

Linked Drug Pages (1)

Potassium Chloride in Dextrose and Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ed62bbc9-60b1-41c1-ae42-846cb79daa11", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X", "IY9XDZ35W2"], "rxcui": ["615099", "615100", "615107", "630796", "1863605", "1863973", "1863988", "1866190"], "spl_set_id": ["59ccc717-c374-41c0-be58-9647df881160"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CONTAINER in 1 CASE (0264-7636-00)  / 1000 mL in 1 CONTAINER", "package_ndc": "0264-7636-00", "marketing_start_date": "19880217"}], "brand_name": "Potassium Chloride in Dextrose and Sodium Chloride", "product_id": "0264-7636_ed62bbc9-60b1-41c1-ae42-846cb79daa11", "dosage_form": "INJECTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0264-7636", "generic_name": "DEXTROSE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Dextrose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE, UNSPECIFIED FORM", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": ".22 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".45 g/100mL"}], "application_number": "NDA019630", "marketing_category": "NDA", "marketing_start_date": "19880217", "listing_expiration_date": "20261231"}