Shenzhen Oriental Pharmaceutical Co.,Ltd.

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+86-571-8627 3270

Shenzhen Oriental Pharmaceutical Co.,Ltd.

29 YRS

Guangdong, China

CNY 20 Million

9990 m²

Less than 50 people

Main Products: Phenylephrine Hydrochloride / Doxylamine Succinate / Phenylephrine Bitartrate / Etilefrine Hydrochloride / L-Adrenaline Brtartrate / Noradrenaline Bitartrate / Isoproterenol Hydrochloride / Epinephrine Hydrochloride / Dorzolamide Hydrochloride / Docusate Sodium / Pseudoephedrine Sulfate

Guangdong, China

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Shenzhen Oriental Pharmaceutical

Specialize in the development, production and sales of distinctive & combined APIs and high-end pharmaceutical intermediates.

VERIFIEDMANUFACTURINGCOMPANY

Business Type

Manufacturing

Total Employees

0-50 People

Plant Size

15 Acres

Production Experience

29+ Years

Registered Capital

CNY 20 Million

MAIN
PRODUCTS

1/3

Phenylephrine HCl

CAS: 61-76-7

Packing: 25 KG/Fibre Drum

Lead Time: 1-2 weeks

Inquiry

1/3

Doxylamine Succinate

CAS: 562-10-7

Specification: USP/EP

Packing: 20 KG/Fibre Drum; 25 KG/Fibre Drum

Lead Time: 14-30 days

Inquiry

1/3

Phenylephrine Bitartrate

CAS: 17162-39-9

Packing: 25 KG/Fibre Drum

Lead Time: 14-30 days

Inquiry

ABOUT US

Shenzhen Oriental Pharmaceutical Co.,Ltd.

Shenzhen Oriental Pharmaceutical Co., Ltd. is one of the subsidiary of Happy Industrial (Hong Kong) Investment Group, established in 1995 and has passed the GMP and US FDA. It is a qualified supplier to many large multinational pharmaceutical companies, specializing in the development, production and sales of distinctive & combined APIs and high-end pharmaceutical intermediates. The main products are Phenylephrine Hcl, Doxylamine succinate and Etilefrine Hcl. The company is equipped with complete production equipment, which can meet various complex chemical reactions from small test, pilot test to large scale production; Equipped with advanced testing equipment, including HPLC, GC and UV equipment; installed sewage and waste gas treatment equipment, Meet the latest environmental requirements. Our products are manufactured in accordance with the most stringent requirements of our customers and health authorities. DMF documentation for all our products is prepared in accordance with the latest requirements of ICH (Eu DMF, CTD), and FDA (US DMF). Materials and product testing is performed in line with the European and United States Pharmacopeias. However, our products can be additionally tested in compliance with the customer’s specifications.