Antiviral & Antiretroviral

RemdesivirThird Party Manufacturing in India

Looking to get Remdesivir manufactured under your brand? Our WHO-GMP certified partner facilities support PCD franchise partners and global export opportunities structured across 25+ countries.

WHO-GMP Certified
Export Ready
PCD Franchise Available
CAS Number
1809249-37-3
Drug Class
Nucleotide analog RNA polymerase inhibitor
Molecular Formula
C₂₇H₃₅N₆O₈P
Molecular Weight
602.6 g/mol
Grade Standards
IP, USP, BP
Therapeutic Category
Antiviral & Antiretroviral
MOQ
Contact us for MOQ
Dosage Forms
Injection (Lyophilized Powder)

Mechanism of Action

Remdesivir works as a broad-spectrum antiviral prodrug that interferes with viral RNA replication. Once administered intravenously, it is taken up by host cells and metabolized through a series of phosphorylation steps into its pharmacologically active form, remdesivir triphosphate, which closely resembles the natural nucleotide adenosine triphosphate (ATP).

This active metabolite acts as a competitive inhibitor of the viral RNA-dependent RNA polymerase (RdRp), the enzyme responsible for copying the viral genetic material. When the viral polymerase attempts to incorporate remdesivir triphosphate into the growing RNA chain instead of ATP, the modified nucleotide is successfully integrated. However, after three to five additional nucleotides are added, the incorporation of remdesivir causes delayed chain termination, effectively halting further elongation of the viral RNA strand. This prevents the virus from completing genome replication and producing new infectious particles.

Remdesivir has demonstrated antiviral activity against multiple families of RNA viruses including coronaviruses, filoviruses, and paramyxoviruses. Its prodrug design enhances intracellular delivery and activation of the active nucleotide, achieving significantly higher intracellular concentrations than the parent nucleoside alone. The drug is primarily metabolized in the liver and excreted via the kidneys.

Therapeutic Uses & Indications

Therapeutic Uses

Remdesivir is indicated for the treatment of:

  • COVID-19 in Hospitalized Patients: Reduces recovery time and prevents disease progression in adults and pediatric patients with SARS-CoV-2 infection who require supplemental oxygen or are at high risk of progressing to severe disease.
  • COVID-19 in Non-Hospitalized High-Risk Patients: Prevents hospitalization and death in patients with mild to moderate COVID-19 who are at high risk of progression, including those with advanced age, obesity, diabetes, or immunosuppression.
  • Coronavirus Infections Beyond SARS-CoV-2: In vitro activity has been demonstrated against SARS-CoV, MERS-CoV, and other coronaviruses, though clinical use remains primarily for COVID-19.

Why Manufacturers Choose Remdesivir

Remdesivir was the first antiviral drug approved by the FDA for COVID-19 and remains a cornerstone therapy for hospitalized patients. Its widespread use during the pandemic established a massive global demand infrastructure that continues to drive procurement by government stockpiles and hospital formularies. The lyophilized powder for injection requires specific aseptic manufacturing capabilities, positioning contract manufacturers with sterile injectable facilities at a premium in the pharmaceutical outsourcing market.

This makes Remdesivir one of the most sought-after molecules for third party manufacturing in India, with consistent demand from export-oriented companies supplying regulated markets.

Dosage Forms We Manufacture

Injection (Lyophilized Powder)
100mg/vial

Frequently Asked Questions

What is the minimum order quantity for Remdesivir?
Minimum order quantity for Remdesivir is Contact us for MOQ. Please contact us for bulk pricing and custom quantities.
What dosage forms of Remdesivir can you manufacture?
We manufacture Remdesivir as: Injection (Lyophilized Powder) (100mg/vial).
Are your manufacturing facilities WHO-GMP certified?
Yes. Celesta Healthcare works exclusively with WHO-GMP certified partner production facilities. All manufacturing batches are subject to strict quality control and documentation.
Can you manufacture Remdesivir for export?
Yes. We provide export-ready Remdesivir formulations structured across 25+ countries. We provide full export documentation including Certificate of Analysis (CoA), Certificate of Origin, and regulatory dossiers on request.
What grade standards do you follow for Remdesivir?
We manufacture Remdesivir to IP, USP, BP pharmacopoeial standards.
Third Party Manufacturing

Get Remdesivir made under your brand

  • WHO-GMP certified facilities
  • Quote within 24 hours
  • MOQ from Contact us for MOQ
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Our Manufacturing Capabilities

  • WHO-GMP Certified Partner Plants
  • 25+ years of pharma industry experience
  • PCD Franchise with monopoly rights
  • Export support across 25+ countries
  • Small batch to commercial scale
  • Custom formulation development

Packaging Options

Single-dose vial with diluent.

Start Manufacturing Remdesivir Today

Celesta Healthcare provides WHO-GMP certified third-party manufacturing for Remdesivir across all dosage forms. PCD franchise and export orders welcome.

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