NDC 0409-8183

Potassium Acetate

Potassium Acetate

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

• Product ID: 0409-8183_28f98aef-8865-4faf-b491-a77b56513d5d
• NDC: 0409-8183
• Product Type: Human Prescription Drug
• Proprietary Name: Potassium Acetate
• Generic Name: Potassium Acetate
• Dosage Form: Injection, Solution, Concentrate
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2014-03-27
• Marketing Category: NDA / NDA
• Application Number: NDA018896
• Labeler Name: Hospira, Inc.
• Substance Name: POTASSIUM ACETATE
• Active Ingredient Strength: 4 g/20mL
• Pharm Classes: 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 Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 0409-8183-25

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-8183-25) > 20 mL in 1 VIAL, SINGLE-DOSE (0409-8183-15)

• Marketing Start Date: 2014-03-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0409-8183-11 [00409818311]

Potassium Acetate INJECTION, SOLUTION, CONCENTRATE

• Marketing Category: NDA
• Application Number: NDA018896
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2017-06-13

NDC 0409-8183-01 [00409818301]

Potassium Acetate INJECTION, SOLUTION, CONCENTRATE

• Marketing Category: NDA
• Application Number: NDA018896
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2005-07-07

NDC 0409-8183-15 [00409818315]

Potassium Acetate INJECTION, SOLUTION, CONCENTRATE

• Marketing Category: NDA
• Application Number: NDA018896
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2017-06-13

NDC 0409-8183-25 [00409818325]

Potassium Acetate INJECTION, SOLUTION, CONCENTRATE

• Marketing Category: NDA
• Application Number: NDA018896
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2014-03-27

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM ACETATE	3.93 g/20mL

OpenFDA Data

• SPL SET ID: c7eabefd-2781-439b-b8f4-cb3ea25a4720
• Manufacturer:
  • Hospira, Inc.
• UNII:
  • M911911U02
• RxNorm Concept Unique ID - RxCUI:
  • 1871155

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]

NDC Crossover Matching brand name "Potassium Acetate" or generic name "Potassium Acetate"

NDC	Brand Name	Generic Name
0409-3294	Potassium Acetate	POTASSIUM ACETATE
0409-8183	Potassium Acetate	POTASSIUM ACETATE
51754-2001	Potassium Acetate	POTASSIUM ACETATE