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Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products. 
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01 Supriya Lifescience (1)
02 Beijing Taiyang Pharmaceutical Industry (1)
03 Catalytica (1)
04 F. Hoffmann-La Roche (1)
05 GLAND PHARMA LIMITED (1)
06 Industriale Chimica s.r.l. (1)
07 KAMUD DRUGS PVT LTD (1)
08 Kongo Chemical Co., Ltd. (1)
09 Qidong Dongyue Pharmaceutical Co., Ltd. (1)
10 Recordati (1)
11 Souvin Pharmaceuticals Pvt. Ltd (1)
12 Unichem Laboratories Limited (2)
13 Wanbury Limited (1)
14 Blank (2)
01 DIPHENHYDRAMINE HCL (1)
02 DIPHENHYDRAMINE HCL & DIMENHYDRINATE (1)
03 DIPHENHYDRAMINE HCL 100MG S.R. CAPSULES (1)
04 DIPHENHYDRAMINE HCL USP (3)
05 DIPHENHYDRAMINE HCL USP XX (1)
06 DIPHENHYDRAMINE HYDROCHLORIDE (6)
07 DIPHENHYDRAMINE HYDROCHLORIDE USP (3)
01 China (2)
02 India (8)
03 Italy (2)
04 Japan (1)
05 Switzerland (1)
06 Blank (2)
01 Active (7)
02 Inactive (9)
01 Complete (6)
02 Blank (10)
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PharmaCompass offers a list of Diphenhydramine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Diphenhydramine Hydrochloride API Price utilized in the formulation of products. Diphenhydramine Hydrochloride API Price is not always fixed or binding as the Diphenhydramine Hydrochloride Price is obtained through a variety of data sources. The Diphenhydramine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300611 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300611, including repackagers and relabelers. The FDA regulates Tox21_300611 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300611 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Tox21_300611 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tox21_300611 supplier is an individual or a company that provides Tox21_300611 active pharmaceutical ingredient (API) or Tox21_300611 finished formulations upon request. The Tox21_300611 suppliers may include Tox21_300611 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_300611 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tox21_300611 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_300611 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_300611 DMFs exist exist since differing nations have different regulations, such as Tox21_300611 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_300611 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_300611 USDMF includes data on Tox21_300611's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_300611 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tox21_300611 suppliers with USDMF on PharmaCompass.
We have 13 companies offering Tox21_300611
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