Lidocaine Base & Lidocaine HCl

Alcon Bioscience offers a wide range of SSPL Units II products which includes Triamcinolone Acetonide. It belongs to Steroids category. Contact us for more information.

Alcon Bioscience offers a wide range of SSPL Units I products which includes Trimetazidine. It belongs to Multi-pupose block category. Contact us for more information.

Alcon Bioscience offers a wide range of Finished dosage veterinary products which includes Vitamin C supplement. It belongs to Equine Nutritional Premixes category. Contact us for more information.

Alcon Bioscience offers a wide range of Finished dosage veterinary products which includes Vitamin E Supplement. It belongs to Equine Nutritional Premixes category. Contact us for more information.

We manufacture the API in our USFDA inspected, EUGMP Certified, Cofepris Mexcio and Korean MFDS approved facility Swati Spentose Pvt Ltd unit 1. We have filed USDMF and also have EU ASMF for this API. ASMF Filed in: Denmark, Germany, Norway, Sweden, Spain, Cyprus, Czech, Hungary, Ireland, Ita...

1. We are manufacturing Melatonin in our facility Swati Spentose Pvt. Ltd. which is a USFDA-inspected, EU-GMP Certified, WHO GMP certified, COFEPRIS Mexico and Korean MFDS-approved facility.

2. We can supply Melatonin USP, BP as well as Melatonin EP

3. We have Written...

Tamsulosin & Silodosin is manufactured at our facility SSPL-1 which is USFDA-inspected, EUGMP Certified, Cofepris Mexico, and Korean FDA-approved facility, which is also WHO-GMP certified and compliant with major regulatory bodies worldwide.
Our regulatory filings status is as below:
...

Glycopyrrolate is manufactured at a USFDA Inspected, EUGMP Certified, Cofepris Mexico, and Korean FDA-approved facility, which is also WHO-GMP certified and compliant with major regulatory bodies worldwide. 

Our regulatory filings details are given below.
USDMF Numbers:

Glyc...

We can offer Meloxicam API in USP, BP, EP, and IP. Our material is under registration in China.
We have the USDMF,  CEP / ASMF, NMPA (China), DIFA (Brazil), MFDS (Korea), COFEPRIS (Mexico), MOH (Russia), SAHPRA (South Africa),WHO GMP

We are proud to offer Silodosin, manufactured in our state-of-the-art facility, which boasts an impressive array of international certifications.

- USFDA inspected
- EU GMP certified
- ANVISA Brazil approved
- COFEPRIS Mexico approved
- Korean MFDS approved
...

We are proud to offer Prilocaine Base, manufactured in our state-of-the-art facility, which boasts an impressive array of international certifications.

- USFDA inspected
- EU GMP certified
- ANVISA Brazil approved
- COFEPRIS Mexico approved
- Korean MFDS approve...

We are proud to offer Prilocaine HCl, manufactured in our state-of-the-art facility, which boasts an impressive array of international certifications.

- USFDA inspected
- EU GMP certified
- ANVISA Brazil approved
- COFEPRIS Mexico approved
- Korean MFDS approved...

We are Swati Spentose Pvt. Ltd. (SSPL), a pharmaceutical company, specializing in manufacturing APIs with backward integration and are also forward integrated into Finished Dosage Forms. Following is our short introduction and product list. Our product list and compliances are given below :

· Unit 1 facility : Facility having approvals/certifications from USFDA, EUGMP, ANVISA (Brazil), WHO GMP, COFEPRIS (Mexico), and Korean MFDS. (AFM Certificate No.: AG12300239).

· Unit 2 facility: A dedicated facility for steroids and hormones. It is PMDA (Japan) inspected and certified by ANVISA (Brazil) and WHO GMP.

· BJPPL: WHO GMP certified and compliant with USFDA and EUGMP.

. Unit 3 facility : This is our finished formulation facility complying with global regulatory standards which will be operational from Q4-2026. 

We are pleased to introduce Swati Spentose Pvt. Ltd., a pharmaceutical company with over four decades of expertise in the development and manufacturing of specialty pharmaceutical products. As part of our strategic expansion, we are pleased to offer Contract Manufacturing (CMO) and Contract Development & Manufacturing (CDMO) services through our newly established, state-of-the-art formulation manufacturing facility.

It has been developed in line with international regulatory standards and incorporates almost  90% automation to ensure consistent product quality, data integrity, and manufacturing efficiency.Our facility has been designed to meet the expectations of global regulated markets & our current manufacturing capabilities include:

Tablets, Hard Gelatin Capsules, Ointments, Creams & Gels, Oral Liquids & Syrups, Sachet Filling & Sealing