API Manufacturers in India
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Active Pharmaceutical Ingredients
Active Pharmaceutical Ingredients (APIs) are the essential components in a medicine that produce the intended therapeutic effect. They are the foundation of every drug formulation, whether generic or branded. As healthcare needs evolve globally, the demand for high-quality APIs has surged across therapeutic categories.
India has emerged as a global hub for API production, known for its cost efficiency, regulatory adherence, and skilled manufacturing ecosystem. At the forefront of this transformation is GCCPL Pharmaceuticals, one of India’s trusted API manufacturers. With a strong commitment to quality, compliance, and innovation, GCCPL delivers a wide range of APIs to pharmaceutical companies worldwide, supporting global healthcare access with consistency and care.
Why Choose GCCPL for API Manufacturing in India?
GCCPL stands out among API manufacturers in India for its robust infrastructure, regulatory strength, and partnership-driven approach. Our facilities are internationally certified, and our processes adhere to stringent global standards, ensuring consistent product quality, traceability, and safety. From early development to commercial-scale supply, we provide customized solutions across therapeutic categories.
WHO-GMP Certified Facilities
Our manufacturing sites are certified by the World Health Organization – Good Manufacturing Practices (WHO-GMP), ensuring that every API we produce meets global benchmarks for quality and safety. Our facilities are equipped with automated systems, advanced lab instrumentation, and continuous process monitoring to deliver reliable and reproducible results.
Regulatory Compliance and Global Standards
At GCCPL, we prioritize full regulatory compliance. Our APIs adhere to US FDA, EU GMP, and other international standards, supported by well-documented DMFs, CoAs, and validation reports. We provide all necessary documentation to support global submissions and streamline regulatory approvals.
Custom Manufacturing Capabilities
GCCPL offers flexible, custom manufacturing services tailored to your needs, whether you’re developing a new molecule or scaling an existing formulation. Our team supports early development, process optimization, and scalable production, delivering efficiency without compromising on compliance or quality.
End-to-End Supply Chain Management
GCCPL offers fully integrated API manufacturing and supply chain capabilities. From raw material sourcing and quality control to warehousing and global distribution, our supply chain ensures on-time delivery and uninterrupted availability of critical APIs.
OUR APIs
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Amikacin Sulphate |
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Amlodipine Besilate |
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Amoxicillin Trihydrate Compacted |
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Azithromycin |
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Alpha Lipoic Acid USP |
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Cefixime Trihydrate |
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Cefpodoxime Proxetil |
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Cefuroxime Axetil |
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Cefoperazone Sodium |
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Ceftriaxone Sodium Sterile |
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Ceftazidime Sterile IP |
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Dextromethorphan HBR |
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Doxycycline Hyclate |
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Ephedrine |
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Levofloxacin Hemihydrate I.P. |
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Pyridoxine Hydrochloride (Vitamin B6) |
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Riboflavin (vitamin B2) I.P. |
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Roxithromycin (MMCPL) |
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Spironolactone I.P.,U.S.P.,E.P. |
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Empagliflozin (Under Development) |
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Alpha Lipoic Acid |
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Levetiracetam IP |
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Levofloxacin |
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Metformin HCL |
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Metronidazole IP |
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Pantaprazole – Sodium IP |
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Piperacillin Sodium+Tazobactam Sodium Sterile – IP |
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Potassium Clavulanate with Avicel (Clavulanic Acid) |
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Potassium Clavulanate with Syloid |
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Pseudoephedrine hcl |
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Progesterone IP (Micronized) |
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Phenylephrine HCL IP |
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Roxithromycin |
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Spironolactone |
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Sulfadimidine |
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Paracetamol I.P.,U.S.P.,E.P. |
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Prednisolone |
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Tetracycline Hydrochloride I.P. |
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Thiamine Hydrochloride (Vitamin B1) |
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Vildagliptin |
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Levonorgestrel |
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Sulphate Glycerin |
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Sulbactam sodium sterile |
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Telmisartan |
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Vitamin B1 HCL – Thiamine HCL |
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Vitamin B1 Mono – Thiamine Mononitrate |
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Vitamin B6 (Pyridoxine HCL) |
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Vitamin B12 (Cyanocobalamin) |
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Vitamin B3 (Niacinamide) |
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Sulfadiazine |
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Dexamethasone I.P., U.S.P., E.P., B.P., |
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Dexamethasone Sodium Phosphate I.P., U.S.P., E.P., B.P. |
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Hydrocortisone I.P.,U.S.P.,E.P |
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Hydrocortisone Acetate I.P.,E.P. |
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Levofloxacin Hemihydrate I.P. |
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Levofloxacin Hemihydrate I.P. |
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Netilmicin sulphate I.P |
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Tobramycin |
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Prednisone |
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Dapagliflozin |
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Obeticholic Acid |
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Neomycin Sulfate |
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Levamisole |
High-Quality API Intermediate Manufacturing
Our end-to-end service offering is also recognized among leading API intermediate manufacturers in India. Intermediates are crucial building blocks in the synthesis of APIs, and their quality directly impacts the consistency and efficacy of the final product.
Our API intermediate manufacturing facilities follow the same rigorous quality practices as our API units. With a focus on scalability and customization, we support both generic and innovative pharmaceutical companies with reliable intermediates for a variety of therapeutic segments. All intermediates are produced under strict process validation, impurity profiling, and documentation protocols to meet both domestic and international regulatory expectations.
Contact GCCPL - Your Trusted API
Manufacturing Partner
Looking for dependable, compliant, and quality-driven API manufacturers in India? GCCPL Pharmaceuticals is ready to support your project, whether it’s for commercial supply, custom development, or strategic partnership. We combine science, scale, and service with our two-decade-long experience to deliver APIs and intermediaries that meet the evolving needs of the global pharma industry.
Please fill out the inquiry form below, and our technical and business development teams will get in touch to understand your requirements and explore how GCCPL can support your API journey, from molecule to market.
Frequently Asked Questions
What is an API manufacturer?
An API manufacturer produces the active pharmaceutical ingredient used in drug formulations to create therapeutic effects.
Who is the manufacturer of API in India?
India has several API producers. GCCPL is among the leading API manufacturers in India, supplying high-quality, compliant APIs globally.
What makes GCCPL one of the trusted API manufacturers in India?
GCCPL’s WHO-GMP-certified facilities, global regulatory compliance, and custom manufacturing capabilities make it a preferred partner in the API space.
Do you offer API intermediates for custom or bulk manufacturing needs?
Yes, GCCPL provides both custom and bulk API intermediate manufacturing solutions tailored to client requirements across therapeutic areas.
Are your active pharma ingredients compliant with international standards?
Absolutely. Our APIs meet US FDA, EU GMP, and WHO-GMP standards and come with complete regulatory documentation.
Why should pharmaceutical companies partner with GCCPL for active pharma ingredients?
GCCPL offers quality, compliance, scalability, and partnership-driven service, making us a reliable API supplier for global pharma companies.
