API : Famotidine

ORCHEV Pharma is from leading manufacturers of Famotidine located in India. Famotidine is manufactured in USFDA, EU-GMP and COFEPRIS approved facility.

Famotidine US-DMF # 36764 & GDUFA DMF Fees Paid, customer ANDA approval received.

CEP 2022-307 from EDQM

Chinese DMF # Y20220000306 registration successful with IDL Status “A

IL# 028647 & TDMF consolidated & approved by Taiwan FDA

Famotidine DMF filed Korean FDA.

Iran MOH Registration

WHO-GMP, WC, DMF, Risk Assessments Reports, etc. are available with ORCHEV.

Famotidine installed production capacity of 10 MT/Month.

All key intermediates of Famotidine are manufactured in-house in our USFDA/EU-GMP approved facility, directly giving us better control of supply chain, quality, and cost.

We are offering commercial supplies of Famotidine intermediates as well. Intermediates being part of our DMF, customers are assured of full documentation, audit, and GMP controls for intermediates as well.

Famotidine is a histamine H2 receptor antagonist medication that decreases stomach acid production. It is used to treat peptic ulcer disease, gastroesophageal reflux disease, and Zollinger-Ellison syndrome. It is taken by mouth or by injection into a vein. It begins working within an hour.

Possible use of Famotidine in COVID-19 is being studied in the US. Few reputed medical journals have reported Famotidine use associated with improved outcomes in COVID-19 patients.

ORCHEV is your trusted Famotidine manufacturing company, having required regulatory documents like GMP, DMF, stability report, etc.

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