potassium chloride in sodium chloride

Generic: sodium chloride and potassium chloride

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride in sodium chloride
Generic Name sodium chloride and potassium chloride
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

potassium chloride 300 mg/100mL, sodium chloride 900 mg/100mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-688
Product ID 63323-688_23c084c3-6c81-4691-9e86-0c2a17df7076
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212347
Listing Expiration 2026-12-31
Marketing Start 2021-06-02

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 63323688
Hyphenated Format 63323-688

Supplemental Identifiers

RxCUI
237367 403890 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 ANDA212347 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 300 mg/100mL
  • 900 mg/100mL
source: ndc
Packaging
  • 10 BAG in 1 CARTON (63323-688-10) / 1000 mL in 1 BAG (63323-688-01)
source: ndc

Packages (1)

63323-688-10 10 BAG in 1 CARTON (63323-688-10) / 1000 mL in 1 BAG (63323-688-01)

Ingredients (2)

potassium chloride (300 mg/100mL) sodium chloride (900 mg/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": "23c084c3-6c81-4691-9e86-0c2a17df7076", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X"], "rxcui": ["237367", "403890", "637551"], "spl_set_id": ["c2467d57-cd2d-4409-bcc0-50128bd01bba"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CARTON (63323-688-10)  / 1000 mL in 1 BAG (63323-688-01)", "package_ndc": "63323-688-10", "marketing_start_date": "20210602"}], "brand_name": "Potassium Chloride in Sodium Chloride", "product_id": "63323-688_23c084c3-6c81-4691-9e86-0c2a17df7076", "dosage_form": "INJECTION, 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": "63323-688", "generic_name": "Sodium Chloride and Potassium Chloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Sodium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "300 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "application_number": "ANDA212347", "marketing_category": "ANDA", "marketing_start_date": "20210602", "listing_expiration_date": "20261231"}