potassium phosphates
Generic: potassium phosphate, monobasic potassium phosphate, dibasic
Labeler: american regent, inc.Drug Facts
Product Profile
Brand Name
potassium phosphates
Generic Name
potassium phosphate, monobasic potassium phosphate, dibasic
Labeler
american regent, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
potassium phosphate, dibasic 236 mg/mL, potassium phosphate, monobasic 224 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0517-2505
Product ID
0517-2505_e76a57d0-94d0-4eed-9969-66f2c553ed5c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216274
Listing Expiration
2026-12-31
Marketing Start
2023-10-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05172505
Hyphenated Format
0517-2505
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 phosphate, monobasic potassium phosphate, dibasic (source: ndc)
Application Number
ANDA216274 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 236 mg/mL
- 224 mg/mL
Packaging
- 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0517-2505-25) / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (0517-2505-01)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e76a57d0-94d0-4eed-9969-66f2c553ed5c", "openfda": {"unii": ["4J9FJ0HL51", "CI71S98N1Z"], "rxcui": ["1928567", "1928569", "2667657"], "spl_set_id": ["41a85cca-c463-4f39-9335-177b04c290a9"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0517-2505-25) / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (0517-2505-01)", "package_ndc": "0517-2505-25", "marketing_start_date": "20231013"}], "brand_name": "Potassium Phosphates", "product_id": "0517-2505_e76a57d0-94d0-4eed-9969-66f2c553ed5c", "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": "0517-2505", "generic_name": "Potassium Phosphate, Monobasic Potassium Phosphate, Dibasic", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Phosphates", "active_ingredients": [{"name": "POTASSIUM PHOSPHATE, DIBASIC", "strength": "236 mg/mL"}, {"name": "POTASSIUM PHOSPHATE, MONOBASIC", "strength": "224 mg/mL"}], "application_number": "ANDA216274", "marketing_category": "ANDA", "marketing_start_date": "20231013", "listing_expiration_date": "20261231"}