About

ABOUT Stallion LABORATORIES

Stallion Headquartered in Ahmedabad (India) along with three Overseas offices in Vietnam, Nigeria and Angola for its international operations.

Stallion manufactures a wide range of pharmaceuticals, across the broad spectrum of therapies which includes Antidiabetics, Cardiovascular, Urology, Antibiotics – Antibacterial, Gastrointestinal, Cough & Cold, Anxiolytics & Antidepressants, Analgesics –Anti-Inflammatories, Antivirals, Antifungals, Anthelminthic, Anti protozoal, Antimalarial, Antihistaminic, Nutritional supplements and others.

Stallion has its’ strong presence in more than 50+ countries across South East Asia, Africa, Latin/central America and CIS regions.

Stallion is crowned with WHO GMP, GLP & ISO 9001-2015 Certifications after successful completion of audit by respective authorities and with their approval (15 authorities approval)

Stallion Laboratories Unit-II is New Ultra-Modern Facility designed for oral solid dosage form in compliance to latest SRA Guidelines and already applied for approval in SRA countries.

MANUFACTURING UNIT-I AT GIDC, BAVLA, AHMEDABAD :

“Manufacturing Unit-I (WHO-GMP certified) produces General Tablets, Capsules , Oral Dry Powder and Oral Liquid Formulations.” 

Manufacturing Capacity:

▪ 1.8 billion of Tablets, Capsules & Sachets

▪ 6 million of Oral Liquids

MANUFACTURING UNIT-II AT GALLOPS INDUSTRIAL PARK, CHACHRAWADI VASNA, AHMEDABAD :

“New Ultra-Modern Facility designed for oral solid dosage form in compliance with Schedule M and considering SRA (Stringent Regulatory Authority) standard.”

▪ Equipped with high end modern machineries and technologies (21 CFR Complied).

▪ OSD Capacity: 2.2 billion with scope of future expansion of additional 2 lines (Capacity 4 billion)

▪ The total area of land is 11,982 Square meters including 11211.51 Square meters built up area.

Accreditation

Stallion… KEY STRENGTHS

REGULATORY AFFAIRS

In house Regulatory team of experienced qualified pharmacist of more than 30 members shall provide ACTD, CTD, E-CTD & Country specific dossier having Dossier bank of more than 400 products

QUALITY CONTROL

Advanced set up of Quality Control facility with Microbiology Lab. (GLP Qualified) With high end sophisticated Instruments like HPLC,GC, AAS , IR …

F&D

Dedicated in-house F & D facility with Analytical Research Lab. For new Products development More than 15 persons team in R & D. Mainly focused on off patent drugs Developed 18 new products in year 2021

CUSTOMER SATISFACTION

In-House facility from Design to Quality Products Delivery with well established Quality Operations to ascertain an utmost satisfaction of our customers.