potassium phosphate

Generic: potassium phosphate

Labeler: somerset therapeutics, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium phosphate
Generic Name potassium phosphate
Labeler somerset therapeutics, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dibasic potassium phosphate 236 mg/mL, monobasic potassium phosphate 224 mg/mL

Manufacturer
Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-746
Product ID 70069-746_d9961ad1-b332-4cfa-8072-6263917b9788
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217726
Listing Expiration 2026-12-31
Marketing Start 2024-07-11

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 70069746
Hyphenated Format 70069-746

Supplemental Identifiers

RxCUI
1928567 1928569
UPC
0370069747254 0370069746257 0370069747018 0370069746011
UNII
4J9FJ0HL51 CI71S98N1Z

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 phosphate (source: ndc)
Generic Name potassium phosphate (source: ndc)
Application Number ANDA217726 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 236 mg/mL
  • 224 mg/mL
source: ndc
Packaging
  • 25 BOTTLE in 1 CARTON (70069-746-25) / 5 mL in 1 BOTTLE
source: ndc

Packages (1)

70069-746-25 25 BOTTLE in 1 CARTON (70069-746-25) / 5 mL in 1 BOTTLE

Ingredients (2)

dibasic potassium phosphate (236 mg/mL) monobasic potassium phosphate (224 mg/mL)

Linked Drug Pages (1)

Potassium Phosphate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "d9961ad1-b332-4cfa-8072-6263917b9788", "openfda": {"upc": ["0370069747254", "0370069746257", "0370069747018", "0370069746011"], "unii": ["4J9FJ0HL51", "CI71S98N1Z"], "rxcui": ["1928567", "1928569"], "spl_set_id": ["52f07402-1869-4a97-9c92-9729dc611f85"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 BOTTLE in 1 CARTON (70069-746-25)  / 5 mL in 1 BOTTLE", "package_ndc": "70069-746-25", "marketing_start_date": "20240711"}], "brand_name": "Potassium Phosphate", "product_id": "70069-746_d9961ad1-b332-4cfa-8072-6263917b9788", "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 Compounds [CS]", "Potassium Salt [EPC]", "Potassium Salt [EPC]"], "product_ndc": "70069-746", "generic_name": "Potassium Phosphate", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Phosphate", "active_ingredients": [{"name": "DIBASIC POTASSIUM PHOSPHATE", "strength": "236 mg/mL"}, {"name": "MONOBASIC POTASSIUM PHOSPHATE", "strength": "224 mg/mL"}], "application_number": "ANDA217726", "marketing_category": "ANDA", "marketing_start_date": "20240711", "listing_expiration_date": "20261231"}