potassium phosphates

Generic: potassium phosphates

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium phosphates
Generic Name potassium phosphates
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

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

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-0032
Product ID 0409-0032_bc88fab4-5971-468e-b2e0-907a4d91899d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217459
Listing Expiration 2026-12-31
Marketing Start 2025-09-29

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 04090032
Hyphenated Format 0409-0032

Supplemental Identifiers

RxCUI
1928569
UNII
CI71S98N1Z 4J9FJ0HL51

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 phosphates (source: ndc)
Generic Name potassium phosphates (source: ndc)
Application Number ANDA217459 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 236 mg/mL
  • 224 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-0032-01) / 15 mL in 1 VIAL, SINGLE-DOSE (0409-0032-10)
source: ndc

Packages (1)

0409-0032-01 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-0032-01) / 15 mL in 1 VIAL, SINGLE-DOSE (0409-0032-10)

Ingredients (2)

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

Linked Drug Pages (1)

Potassium Phosphates ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "bc88fab4-5971-468e-b2e0-907a4d91899d", "openfda": {"unii": ["CI71S98N1Z", "4J9FJ0HL51"], "rxcui": ["1928569"], "spl_set_id": ["2fcbc814-c7a4-469a-8b1d-6819b961bfb9"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-0032-01)  / 15 mL in 1 VIAL, SINGLE-DOSE (0409-0032-10)", "package_ndc": "0409-0032-01", "marketing_start_date": "20250929"}], "brand_name": "Potassium Phosphates", "product_id": "0409-0032_bc88fab4-5971-468e-b2e0-907a4d91899d", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "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": "0409-0032", "generic_name": "potassium phosphates", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Phosphates", "active_ingredients": [{"name": "DIBASIC POTASSIUM PHOSPHATE", "strength": "236 mg/mL"}, {"name": "MONOBASIC POTASSIUM PHOSPHATE", "strength": "224 mg/mL"}], "application_number": "ANDA217459", "marketing_category": "ANDA", "marketing_start_date": "20250929", "listing_expiration_date": "20261231"}