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Generated: April 19, 2019

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 206759

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NDA 206759 describes POTASSIUM CHLORIDE, which is a drug marketed by Actavis Labs Fl Inc, Adare Pharms Inc, Amneal Pharms, Anchen Pharms, Glenmark Pharms Ltd, Lannett Co Inc, Lupin Ltd, Nesher Pharms, Novel Labs Inc, Paddock Llc, PII, Teva, Tris Pharma Inc, Zydus Pharms Usa Inc, Epic Pharma Llc, Pharma Res Software, Abraxis Pharm, Akorn, B Braun, Baxter Hlthcare, Fresenius Kabi Usa, Gd Searle Llc, Hospira, Intl Medication, Lilly, Luitpold, Miles, Pharma Serve Ny, Watson Labs, Amneal Pharms Llc, Apotex Inc, Genus Lifesciences, Aurobindo Pharma Ltd, Copley Pharm, Mylan Pharms Inc, Schering, Sigmapharm Labs Llc, Strides Pharma, Vitruvias Therap, Yichang Humanwell, and Icu Medical Inc, and is included in eighty-seven NDAs. It is available from fifty-seven suppliers. Additional details are available on the POTASSIUM CHLORIDE profile page.

The generic ingredient in POTASSIUM CHLORIDE is calcium chloride; dextrose; potassium chloride; sodium chloride; sodium lactate. There are two hundred and eighty-two drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the calcium chloride; dextrose; potassium chloride; sodium chloride; sodium lactate profile page.
Summary for 206759
Tradename:POTASSIUM CHLORIDE
Applicant:Novel Labs Inc
Ingredient:potassium chloride
Patents:0
Formulation / Manufacturing:see details
Suppliers and Packaging for NDA: 206759
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
POTASSIUM CHLORIDE potassium chloride TABLET, EXTENDED RELEASE;ORAL 206759 ANDA Novel Laboratories, Inc. 40032-912 40032-912-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (40032-912-01)
POTASSIUM CHLORIDE potassium chloride TABLET, EXTENDED RELEASE;ORAL 206759 ANDA Novel Laboratories, Inc. 40032-912 40032-912-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (40032-912-05)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength8MEQ
Approval Date:Aug 9, 2016TE:AB2RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength10MEQ
Approval Date:Aug 9, 2016TE:AB2RLD:No

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