potassium chloride in dextrose

Generic: dextrose 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
Generic Name dextrose and potassium chloride
Labeler b. braun medical inc.
Dosage Form SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose 5 g/100mL, potassium chloride .15 g/100mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-7625
Product ID 0264-7625_7e397c6d-62c4-4aa0-b19d-d01c5ac6d868
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019699
Listing Expiration 2026-12-31
Marketing Start 1989-09-29

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 02647625
Hyphenated Format 0264-7625

Supplemental Identifiers

RxCUI
309783 309786
UNII
IY9XDZ35W2 660YQ98I10

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 (source: ndc)
Generic Name dextrose and potassium chloride (source: ndc)
Application Number NDA019699 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • .15 g/100mL
source: ndc
Packaging
  • 12 CONTAINER in 1 CASE (0264-7625-00) / 1000 mL in 1 CONTAINER
source: ndc

Packages (1)

0264-7625-00 12 CONTAINER in 1 CASE (0264-7625-00) / 1000 mL in 1 CONTAINER

Ingredients (2)

dextrose (5 g/100mL) potassium chloride (.15 g/100mL)

Linked Drug Pages (1)

POTASSIUM CHLORIDE IN DEXTROSE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "7e397c6d-62c4-4aa0-b19d-d01c5ac6d868", "openfda": {"unii": ["IY9XDZ35W2", "660YQ98I10"], "rxcui": ["309783", "309786"], "spl_set_id": ["e5bbb3e1-ab50-4ec7-a2b4-ce4091712e23"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CONTAINER in 1 CASE (0264-7625-00)  / 1000 mL in 1 CONTAINER", "package_ndc": "0264-7625-00", "marketing_start_date": "19890929"}], "brand_name": "POTASSIUM CHLORIDE IN DEXTROSE", "product_id": "0264-7625_7e397c6d-62c4-4aa0-b19d-d01c5ac6d868", "dosage_form": "SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0264-7625", "generic_name": "DEXTROSE and POTASSIUM CHLORIDE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE IN DEXTROSE", "active_ingredients": [{"name": "DEXTROSE", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": ".15 g/100mL"}], "application_number": "NDA019699", "marketing_category": "NDA", "marketing_start_date": "19890929", "listing_expiration_date": "20261231"}