Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmalabs
02 1Bakul Group
03 1CSPC New Nova Pharmaceutical
04 1CSPC Pharmaceutical Group
05 1Jilin Shulan Synthetic Pharmaceutical Co.,Ltd.
06 2Roche Diagnostics GmbH
07 1S.S.Pharmachem
08 1Shandong Xinhua Pharmaceutical
09 2Siegfried AG
10 1Sneha Medicare Pvt Ltd
11 1Yashiro Pharmaceutical Co Ltd
01 4China
02 2Germany
03 4India
04 2Switzerland
05 1Blank
01 2Inactive
02 11Blank
01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
04 9Blank
01 1222MF10082
02 12Blank
01 13Blank
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3962
Submission : 1980-09-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3966
Submission : 1980-09-26
Status : Inactive
Type : II
NDC Package Code : 58624-0544
Start Marketing Date : 1983-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R0-CEP 2007-345 - Rev 01
Issue Date : 2010-02-09
Type : Chemical
Substance Number : 300
Status : Withdrawn by EDQM F...
Certificate Number : R1-CEP 2004-140 - Rev 00
Issue Date : 2011-09-19
Type : Chemical
Substance Number : 300
Status : Withdrawn by Holder
Certificate Number : R1-CEP 2007-288 - Rev 01
Issue Date : 2015-12-15
Type : Chemical
Substance Number : 300
Status : Valid
NDC Package Code : 65724-4519
Start Marketing Date : 2006-03-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2007-289 - Rev 01
Issue Date : 2015-12-15
Type : Chemical
Substance Number : 301
Status : Valid
NDC Package Code : 65724-4519
Start Marketing Date : 2006-03-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Aminophylline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aminophylline, including repackagers and relabelers. The FDA regulates Aminophylline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aminophylline 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 Aminophylline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aminophylline supplier is an individual or a company that provides Aminophylline active pharmaceutical ingredient (API) or Aminophylline finished formulations upon request. The Aminophylline suppliers may include Aminophylline API manufacturers, exporters, distributors and traders.
click here to find a list of Aminophylline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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