potassium phosphates
Generic: potassium phosphates
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
potassium phosphates
Generic Name
potassium phosphates
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dibasic potassium phosphate 4.72 mg/mL, monobasic potassium phosphate 4.48 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65219-658
Product ID
65219-658_b813e96f-27c8-4bb1-ba28-6319ee823a14
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA212832
Listing Expiration
2026-12-31
Marketing Start
2025-06-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219658
Hyphenated Format
65219-658
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 phosphates (source: ndc)
Generic Name
potassium phosphates (source: ndc)
Application Number
NDA212832 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4.72 mg/mL
- 4.48 mg/mL
Packaging
- 30 POUCH in 1 CARTON (65219-658-25) / 1 BAG in 1 POUCH (65219-658-01) / 250 mL in 1 BAG
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b813e96f-27c8-4bb1-ba28-6319ee823a14", "openfda": {"unii": ["4J9FJ0HL51", "CI71S98N1Z"], "rxcui": ["2688947", "2716829"], "spl_set_id": ["357c3020-ea6f-4401-a2e7-cebb82b03144"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (65219-658-25) / 1 BAG in 1 POUCH (65219-658-01) / 250 mL in 1 BAG", "package_ndc": "65219-658-25", "marketing_start_date": "20250615"}], "brand_name": "Potassium Phosphates", "product_id": "65219-658_b813e96f-27c8-4bb1-ba28-6319ee823a14", "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": "65219-658", "generic_name": "Potassium Phosphates", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Phosphates", "active_ingredients": [{"name": "DIBASIC POTASSIUM PHOSPHATE", "strength": "4.72 mg/mL"}, {"name": "MONOBASIC POTASSIUM PHOSPHATE", "strength": "4.48 mg/mL"}], "application_number": "NDA212832", "marketing_category": "NDA", "marketing_start_date": "20250615", "listing_expiration_date": "20261231"}