potassium phosphates

Generic: potassium phosphates in sodium chloride

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium phosphates
Generic Name potassium phosphates in sodium chloride
Labeler amneal pharmaceuticals llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

potassium phosphate, dibasic 4.72 mg/mL, potassium phosphate, monobasic 4.48 mg/mL

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 70121-1722
Product ID 70121-1722_def7f258-3637-4362-b77d-e16904796cd5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA218343
Listing Expiration 2026-12-31
Marketing Start 2024-07-30

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 701211722
Hyphenated Format 70121-1722

Supplemental Identifiers

RxCUI
2688947
UPC
0370121172291
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 in sodium chloride (source: ndc)
Application Number NDA218343 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 4.72 mg/mL
  • 4.48 mg/mL
source: ndc
Packaging
  • 24 POUCH in 1 CARTON (70121-1722-9) / 1 BAG in 1 POUCH / 250 mL in 1 BAG
source: ndc

Packages (1)

70121-1722-9 24 POUCH in 1 CARTON (70121-1722-9) / 1 BAG in 1 POUCH / 250 mL in 1 BAG

Ingredients (2)

potassium phosphate, dibasic (4.72 mg/mL) potassium phosphate, monobasic (4.48 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": "def7f258-3637-4362-b77d-e16904796cd5", "openfda": {"upc": ["0370121172291"], "unii": ["CI71S98N1Z", "4J9FJ0HL51"], "rxcui": ["2688947"], "spl_set_id": ["dce22c93-aa48-48a9-ac8b-716400d33c9e"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CARTON (70121-1722-9)  / 1 BAG in 1 POUCH / 250 mL in 1 BAG", "package_ndc": "70121-1722-9", "marketing_start_date": "20240730"}], "brand_name": "POTASSIUM PHOSPHATES", "product_id": "70121-1722_def7f258-3637-4362-b77d-e16904796cd5", "dosage_form": "INJECTION", "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": "70121-1722", "generic_name": "Potassium Phosphates in sodium chloride", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM PHOSPHATES", "active_ingredients": [{"name": "POTASSIUM PHOSPHATE, DIBASIC", "strength": "4.72 mg/mL"}, {"name": "POTASSIUM PHOSPHATE, MONOBASIC", "strength": "4.48 mg/mL"}], "application_number": "NDA218343", "marketing_category": "NDA", "marketing_start_date": "20240730", "listing_expiration_date": "20261231"}