TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.

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01 1Transo-Pharm USA LLC
02 1LGM Pharma
03 1Laboratorium Ofichem B.V
04 1Noramco
05 3Purisys LLC
06 1Basic Nutrition
07 1AK AND MN BIOFARM CO LTD
08 1Benuvia
09 1Benuvia Therapeutics
10 1Bionorica SE
11 1Canexis Pharma
12 4Catalent Pharma Solutions
13 1Chemport Inc
14 2Curia
15 1Gelita Health GmbH
16 1Jubilant HollisterStier
17 1Mallinckrodt Pharmaceuticals
18 1MediPharm Labs
19 1NATIONAL CENTER FOR NATURAL PRODUCTS RESEARCH
20 1National Institute on Drug Abuse
21 1Norac Pharma
22 1Resolution Chemicals Limited
23 1S AND B PHARMA INC DBA NORAC PHARMA
24 1Sichuan Gowell Pharmaceutical
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01 1Canada
02 2China
03 2Germany
04 1Ireland
05 1Netherlands
06 1South Korea
07 1Switzerland
08 19U.S.A
09 2United Kingdom
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01 14Active
02 7Inactive
03 9Blank
01 2Valid
02 28Blank
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19335
Submission : 2006-04-07
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-06-28
Pay. Date : 2022-06-23
DMF Number : 20682
Submission : 2007-07-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36220
Submission : 2021-10-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1631
Submission : 1971-01-05
Status : Active
Type : II

GDUFA
DMF Review : Reviewed
Rev. Date : 2016-06-03
Pay. Date : 2016-01-29
DMF Number : 30196
Submission : 2016-02-09
Status : Active
Type : II

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A MaxEPA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MaxEPA, including repackagers and relabelers. The FDA regulates MaxEPA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MaxEPA API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A MaxEPA supplier is an individual or a company that provides MaxEPA active pharmaceutical ingredient (API) or MaxEPA finished formulations upon request. The MaxEPA suppliers may include MaxEPA API manufacturers, exporters, distributors and traders.
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We have 24 companies offering MaxEPA
Get in contact with the supplier of your choice: