potassium phosphates
Generic: potassium phosphate, monobasic potassium phosphate, dibasic injection,
Labeler: amneal pharmaceuticals private limitedDrug Facts
Product Profile
Brand Name
potassium phosphates
Generic Name
potassium phosphate, monobasic potassium phosphate, dibasic injection,
Labeler
amneal pharmaceuticals private limited
Dosage Form
SOLUTION, CONCENTRATE
Routes
Active Ingredients
potassium phosphate, dibasic 236 mg/mL, potassium phosphate, monobasic 224 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
80830-1691
Product ID
80830-1691_9256cc7f-e593-4224-8b44-19e8d01d2cb4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216344
Listing Expiration
2026-12-31
Marketing Start
2025-07-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
808301691
Hyphenated Format
80830-1691
Supplemental Identifiers
RxCUI
UPC
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 injection, (source: ndc)
Application Number
ANDA216344 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 236 mg/mL
- 224 mg/mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (80830-1691-9) / 15 mL in 1 VIAL, SINGLE-DOSE (80830-1691-3)
Packages (1)
Ingredients (2)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9256cc7f-e593-4224-8b44-19e8d01d2cb4", "openfda": {"upc": ["0380830169192"], "unii": ["CI71S98N1Z", "4J9FJ0HL51"], "rxcui": ["1928569"], "spl_set_id": ["125121b8-bc4c-44ee-906e-e72f652a5aa6"], "manufacturer_name": ["Amneal Pharmaceuticals Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (80830-1691-9) / 15 mL in 1 VIAL, SINGLE-DOSE (80830-1691-3)", "package_ndc": "80830-1691-9", "marketing_start_date": "20250709"}], "brand_name": "POTASSIUM PHOSPHATES", "product_id": "80830-1691_9256cc7f-e593-4224-8b44-19e8d01d2cb4", "dosage_form": "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": "80830-1691", "generic_name": "potassium phosphate, monobasic potassium phosphate, dibasic injection,", "labeler_name": "Amneal Pharmaceuticals Private Limited", "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": "ANDA216344", "marketing_category": "ANDA", "marketing_start_date": "20250709", "listing_expiration_date": "20261231"}