NDC 0409-7295

Potassium Phosphates

Potassium Phosphate, Monobasic And Potassium Phosphate, Dibasic

Potassium Phosphates is a Intravenous Injection, Solution, Concentrate in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Dibasic Potassium Phosphate; Monobasic Potassium Phosphate.

• Product ID: 0409-7295_8753477e-92ac-49ec-ae5f-1bea5cfaac0b
• NDC: 0409-7295
• Product Type: Human Prescription Drug
• Proprietary Name: Potassium Phosphates
• Generic Name: Potassium Phosphate, Monobasic And Potassium Phosphate, Dibasic
• Dosage Form: Injection, Solution, Concentrate
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2005-08-26
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Hospira, Inc.
• Substance Name: DIBASIC POTASSIUM PHOSPHATE; MONOBASIC POTASSIUM PHOSPHATE
• Active Ingredient Strength: 236 mg/mL; mg/mL
• Pharm 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]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0409-7295-01

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7295-01) > 15 mL in 1 VIAL, SINGLE-DOSE (0409-7295-11)

• Marketing Start Date: 2005-08-26
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0409-7295-27 [00409729527]

Potassium Phosphates INJECTION, SOLUTION, CONCENTRATE

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-07-01
• Marketing End Date: 2014-07-01

NDC 0409-7295-17 [00409729517]

Potassium Phosphates INJECTION, SOLUTION, CONCENTRATE

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-07-01
• Marketing End Date: 2014-07-01

NDC 0409-7295-11 [00409729511]

Potassium Phosphates INJECTION, SOLUTION, CONCENTRATE

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2017-07-13

NDC 0409-7295-01 [00409729501]

Potassium Phosphates INJECTION, SOLUTION, CONCENTRATE

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2005-08-26

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM PHOSPHATE, MONOBASIC	224 mg/mL

OpenFDA Data

• SPL SET ID: d0e359fe-a90b-44e2-960c-cd82babc4f4c
• Manufacturer:
  • Hospira, Inc.
• UNII:
  • 4J9FJ0HL51
  • CI71S98N1Z
• RxNorm Concept Unique ID - RxCUI:
  • 1928569

Pharmacological Class

• Potassium Compounds [CS]
• Potassium Salt [EPC]
• Osmotic Laxative [EPC]
• Increased Large Intestinal Motility [PE]
• Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
• Osmotic Activity [MoA]
• Potassium Compounds [CS]
• Potassium Salt [EPC]
• Osmotic Laxative [EPC]
• Increased Large Intestinal Motility [PE]
• Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
• Osmotic Activity [MoA]

NDC Crossover Matching brand name "Potassium Phosphates" or generic name "Potassium Phosphate, Monobasic And Potassium Phosphate, Dibasic"

NDC	Brand Name	Generic Name
0409-7295	Potassium Phosphates	POTASSIUM PHOSPHATE, MONOBASIC and POTASSIUM PHOSPHATE, DIBASIC
46287-024	POTASSIUM PHOSPHATES	monobasic potassium phosphate and dibasic potassium phosphate
63323-086	Potassium Phosphates	POTASSIUM PHOSPHATE, MONOBASIC and POTASSIUM PHOSPHATE, DIBASIC
65219-052	Potassium Phosphates	Potassium Phosphate, Monobasic Potassium Phosphate, Dibasic
65219-054	Potassium Phosphates	Potassium Phosphate, Monobasic Potassium Phosphate, Dibasic
65219-056	Potassium Phosphates	Potassium Phosphate, Monobasic Potassium Phosphate, Dibasic