DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1Neuland Laboratories Limited
03 1ALMON HEALTHCARE PRIVATE LIMITED
04 1Aragen Life Sciences Limited
05 1Aurobindo Pharma Limited
06 1CHONGQING HUAPONT SHENGCHEM PHARM. CO., LTD.
07 1Chromo Laboratories India Private Limited
08 1DARMERICA, LLC
09 1HETERO DRUGS LIMITED
10 1Hetero Drugs Limited
11 1Hunan Jiudian Pharmaceutical Co.,Ltd.
12 2MSN Pharmachem Private Limited
13 1Professional Compounding Centers of America
14 2Professional Compounding Centers of America dba PCCA
15 1Spectrum Laboratory Products, Inc.
16 1YiChang HEC ChangJiang Pharmaceutical Co., Ltd.
01 1MOXIFLOXACIN HYDRDOCHLORIDE
02 3MOXIFLOXACIN HYDROCHLORIDE
03 1Moxifloxacin
04 3Moxifloxacin HCl
05 7Moxifloxacin Hydrochloride
06 2Moxifloxacin Hydrochloride Monohydrate
07 1moxifloxacin hydrochloride
01 3China
02 9India
03 2U.S.A
04 3United Kingdom
05 1Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-064
Start Marketing Date : 2012-07-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-0131
Start Marketing Date : 2017-12-13
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 29967-0005
Start Marketing Date : 2018-02-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48943-0024
Start Marketing Date : 2002-11-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49587-106
Start Marketing Date : 2014-12-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49574-522
Start Marketing Date : 2019-04-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50370-0001
Start Marketing Date : 2010-04-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
NDC Package Code : 50370-0002
Start Marketing Date : 2010-04-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0089
Start Marketing Date : 2020-09-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-4770
Start Marketing Date : 2020-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Moxifloxacin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Moxifloxacin Hydrochloride, including repackagers and relabelers. The FDA regulates Moxifloxacin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Moxifloxacin Hydrochloride 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 Moxifloxacin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Moxifloxacin Hydrochloride supplier is an individual or a company that provides Moxifloxacin Hydrochloride active pharmaceutical ingredient (API) or Moxifloxacin Hydrochloride finished formulations upon request. The Moxifloxacin Hydrochloride suppliers may include Moxifloxacin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Moxifloxacin Hydrochloride 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 Moxifloxacin Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Moxifloxacin Hydrochloride 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 Moxifloxacin Hydrochloride 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 Moxifloxacin Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Moxifloxacin Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Moxifloxacin Hydrochloride suppliers with NDC on PharmaCompass.
We have 13 companies offering Moxifloxacin Hydrochloride
Get in contact with the supplier of your choice:
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