potassium chloride in sodium chloride

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

potassium chloride .15 g/100mL, sodium chloride .9 g/100mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-7865
Product ID 0264-7865_e0246dd9-bd3e-4e0d-bec9-cd6daf46683d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019708
Listing Expiration 2027-12-31
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 02647865
Hyphenated Format 0264-7865

Supplemental Identifiers

RxCUI
637551
UNII
660YQ98I10 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 potassium chloride in sodium chloride (source: ndc)
Generic Name sodium chloride and potassium chloride (source: ndc)
Application Number NDA019708 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .15 g/100mL
  • .9 g/100mL
source: ndc
Packaging
  • 12 CONTAINER in 1 CASE (0264-7865-00) / 1000 mL in 1 CONTAINER
source: ndc

Packages (1)

0264-7865-00 12 CONTAINER in 1 CASE (0264-7865-00) / 1000 mL in 1 CONTAINER

Ingredients (2)

potassium chloride (.15 g/100mL) sodium chloride (.9 g/100mL)

Linked Drug Pages (1)

POTASSIUM CHLORIDE IN SODIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "e0246dd9-bd3e-4e0d-bec9-cd6daf46683d", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X"], "rxcui": ["637551"], "spl_set_id": ["ecc38772-246a-46c4-b42a-b9b81124f27f"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CONTAINER in 1 CASE (0264-7865-00)  / 1000 mL in 1 CONTAINER", "package_ndc": "0264-7865-00", "marketing_start_date": "19890929"}], "brand_name": "POTASSIUM CHLORIDE IN SODIUM CHLORIDE", "product_id": "0264-7865_e0246dd9-bd3e-4e0d-bec9-cd6daf46683d", "dosage_form": "SOLUTION", "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": "0264-7865", "generic_name": "SODIUM CHLORIDE and POTASSIUM CHLORIDE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE IN SODIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": ".15 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".9 g/100mL"}], "application_number": "NDA019708", "marketing_category": "NDA", "marketing_start_date": "19890929", "listing_expiration_date": "20271231"}