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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 209922
Company: PRINSTON INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription AB1 No No
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 15MEQ TABLET, EXTENDED RELEASE;ORAL Prescription AB1 No No
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription AB1 No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
04/30/2019 ORIG-1 Approval STANDARD

Label is not available on this site.

POTASSIUM CHLORIDE

TABLET, EXTENDED RELEASE;ORAL; 10MEQ
TE Code = AB1

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
KLOR-CON M10 POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 074726 UPSHER SMITH LABS
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 075604 ACTAVIS LABS FL INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 076368 ADARE PHARMS INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 212861 AMNEAL
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 214395 AMTA
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 214422 ASCENT PHARMS INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 203562 GLENMARK PHARMS LTD
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 214452 GRANULES
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 206347 NOVEL LABS INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 209922 PRINSTON INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 10MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 210395 ZYDUS PHARMS

TABLET, EXTENDED RELEASE;ORAL; 15MEQ
TE Code = AB1

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
KLOR-CON M15 POTASSIUM CHLORIDE 15MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 074726 UPSHER SMITH LABS
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 15MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 214422 ASCENT PHARMS INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 15MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 209922 PRINSTON INC

TABLET, EXTENDED RELEASE;ORAL; 20MEQ
TE Code = AB1

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
KLOR-CON M20 POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 074726 UPSHER SMITH LABS
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 075604 ACTAVIS LABS FL INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 076368 ADARE PHARMS INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 212861 AMNEAL
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 214395 AMTA
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 214422 ASCENT PHARMS INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 203562 GLENMARK PHARMS LTD
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 214452 GRANULES
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 206347 NOVEL LABS INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 209922 PRINSTON INC
POTASSIUM CHLORIDE POTASSIUM CHLORIDE 20MEQ TABLET, EXTENDED RELEASE;ORAL Prescription No AB1 210395 ZYDUS PHARMS
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