Aspen API. More than just an API.
01 1Aspen API
02 1Aarti Pharmalabs
03 1TAPI Technology & API Services
04 1Cipla
05 1FDC
06 1Sifavitor srl
07 1Sun Pharmaceutical Industries Limited
Aspen API. More than just an API.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18236
Submission : 2005-04-01
Status :
Type : II
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : Complete
Rev. Date : 2013-03-07
Pay. Date : 2013-02-14
DMF Number : 20557
Submission : 2007-05-23
Status :
Type : II
TAPI offers customized CDMO Solutions for API development and manufacturing services.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18433
Submission : 2005-06-16
Status :
Type : II
A Levalbuterol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levalbuterol Hydrochloride, including repackagers and relabelers. The FDA regulates Levalbuterol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levalbuterol 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 Levalbuterol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levalbuterol Hydrochloride supplier is an individual or a company that provides Levalbuterol Hydrochloride active pharmaceutical ingredient (API) or Levalbuterol Hydrochloride finished formulations upon request. The Levalbuterol Hydrochloride suppliers may include Levalbuterol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Levalbuterol Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levalbuterol Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Levalbuterol Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Levalbuterol Hydrochloride DMFs exist exist since differing nations have different regulations, such as Levalbuterol Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Levalbuterol Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Levalbuterol Hydrochloride USDMF includes data on Levalbuterol Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Levalbuterol Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Levalbuterol Hydrochloride suppliers with USDMF on PharmaCompass.
We have 7 companies offering Levalbuterol Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
