Details for New Drug Application (NDA): 018896
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The generic ingredient in POTASSIUM ACETATE is potassium acetate. There are two hundred and forty drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the potassium acetate profile page.
Summary for 018896
Tradename: | POTASSIUM ACETATE |
Applicant: | Hospira |
Ingredient: | potassium acetate |
Patents: | 0 |
Pharmacology for NDA: 018896
Mechanism of Action | Osmotic Activity |
Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 018896
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
POTASSIUM ACETATE | potassium acetate | INJECTABLE;INJECTION | 018896 | NDA | Hospira, Inc. | 0409-3294 | 0409-3294-25 | 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0409-3294-25) / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-3294-15) |
POTASSIUM ACETATE | potassium acetate | INJECTABLE;INJECTION | 018896 | NDA | Hospira, Inc. | 0409-3294 | 0409-3294-51 | 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0409-3294-51) / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-3294-61) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2MEQ/ML | ||||
Approval Date: | Jul 20, 1984 | TE: | AP | RLD: | Yes |
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