Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience
02 1Malladi Drugs & Pharmaceuticals Limited
03 1Virupaksha Organics
04 2Aurobindo Pharma Limited
05 1Dasami Lab
06 1Divis Laboratories
07 1Exemed Pharmaceuticals
08 1Hy-Gro Chemicals Pharmtek
09 1Lonza Inc & Lonza America Inc
10 1Qidong Dongyue Pharmaceutical Co., Ltd.
11 1Royal DSM
12 1SIGMA TAU
13 1Solara Active Pharma Sciences
14 1Srini Pharmaceuticals
15 1Standard Chem. & Pharm. Co., Ltd
16 1Wanbury Limited
17 1Wockhardt
18 1Zhejiang Apeloa Kangyu Pharmaceutical Co. Ltd
19 2Blank
01 15% D-METHORPHAN HYDROBROMIDE ADSORBATE POWDER
02 1DEXTROMETHOPHAN HYDROBROMIDE
03 7DEXTROMETHORPHAN HYDROBROMIDE
04 1DEXTROMETHORPHAN HYDROBROMIDE (IN BULK TIME RELEASE PELLETIZED FORM)
05 1DEXTROMETHORPHAN HYDROBROMIDE MONOHYDRATE, USP
06 9DEXTROMETHORPHAN HYDROBROMIDE USP
07 1DEXTROMETHORPHAN POLISTIREX
01 3China
02 13India
03 1Netherlands
04 2U.S.A
05 2Blank
01 16Active
02 5Inactive
01 9Complete
02 12Blank
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33575
Submission : 2019-03-25
Status : Active
Type : II
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
GDUFA
DMF Review : Complete
Rev. Date : 2019-05-28
Pay. Date : 2019-04-25
DMF Number : 32402
Submission : 2018-01-04
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-08-23
Pay. Date : 2024-08-19
DMF Number : 39295
Submission : 2024-01-23
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-07-01
Pay. Date : 2014-02-18
DMF Number : 27959
Submission : 2014-02-13
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-09
Pay. Date : 2012-11-23
DMF Number : 12356
Submission : 1997-02-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27836
Submission : 2013-12-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 395
Submission : 1960-08-10
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26762
Submission : 2012-12-26
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2021-09-21
Pay. Date : 2021-07-29
DMF Number : 32848
Submission : 2018-06-04
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-05-16
Pay. Date : 2013-05-09
DMF Number : 11935
Submission : 1996-04-18
Status : Active
Type : II
A Dextromethorphan Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextromethorphan Hydrobromide, including repackagers and relabelers. The FDA regulates Dextromethorphan Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextromethorphan Hydrobromide 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 Dextromethorphan Hydrobromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dextromethorphan Hydrobromide supplier is an individual or a company that provides Dextromethorphan Hydrobromide active pharmaceutical ingredient (API) or Dextromethorphan Hydrobromide finished formulations upon request. The Dextromethorphan Hydrobromide suppliers may include Dextromethorphan Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Dextromethorphan Hydrobromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dextromethorphan Hydrobromide DMF (Drug Master File) is a document detailing the whole manufacturing process of Dextromethorphan Hydrobromide active pharmaceutical ingredient (API) in detail. Different forms of Dextromethorphan Hydrobromide DMFs exist exist since differing nations have different regulations, such as Dextromethorphan Hydrobromide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dextromethorphan Hydrobromide DMF submitted to regulatory agencies in the US is known as a USDMF. Dextromethorphan Hydrobromide USDMF includes data on Dextromethorphan Hydrobromide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dextromethorphan Hydrobromide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dextromethorphan Hydrobromide suppliers with USDMF on PharmaCompass.
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