Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience Limited
02 1Malladi Drugs & Pharmaceuticals Limited
03 1AZEEMA PHARMA INC
04 2Aurobindo Pharma Limited
05 1Dasami Lab Private Limited
06 1Divi's Laboratories Limited
07 1Exemed Pharmaceuticals
08 1HY-GRO CHEMICALS PHARMTEK PVT LTD
09 1Kreative Organics Private Limited
10 1LETCO MEDICAL, LLC
11 1Medisca Inc.
12 1Professional Compounding Centers of America
13 1QIDONG DONGYUE PHARMACEUTICAL CO., LTD.
14 1Spectrum Laboratory Products, Inc.
15 1Srini Pharmaceuticals Private Limited
16 1Vasudha Pharma Chem Limited
17 1Wanbury Limited
18 1Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.
19 1Zhejiang Bamboo Pharmaceuticals Co.,Ltd
01 5DEXTROMETHORPHAN HYDROBROMIDE
02 13Dextromethorphan Hydrobromide
03 1Dextromethorphan Polistirex
04 1Dextromethorphan hydrobromide
01 3China
02 12India
03 4U.S.A
04 1United Kingdom
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-6500
Start Marketing Date : 2017-01-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
NDC Package Code : 57218-760
Start Marketing Date : 2017-02-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-769
Start Marketing Date : 2024-01-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/50kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62331-003
Start Marketing Date : 2002-01-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60155-002
Start Marketing Date : 2020-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58793-004
Start Marketing Date : 2013-06-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0355
Start Marketing Date : 2015-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0260
Start Marketing Date : 2022-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-2500
Start Marketing Date : 1990-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62350-0081
Start Marketing Date : 2019-08-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Dextromethorphan Hydrobromide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dextromethorphan Hydrobromide API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Dextromethorphan Hydrobromide as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Dextromethorphan Hydrobromide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dextromethorphan Hydrobromide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dextromethorphan Hydrobromide suppliers with NDC on PharmaCompass.
We have 19 companies offering Dextromethorphan Hydrobromide
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
