Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.

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01 1Malladi Drugs & Pharmaceuticals Limited
02 1Transo-Pharm USA LLC
03 1LGM Pharma
04 1Laboratorium Ofichem B.V
05 1Noramco
06 3Purisys LLC
07 1Basic Nutrition
08 1AK AND MN BIOFARM CO LTD
09 1Benuvia
10 1Benuvia Therapeutics
11 1Bionorica SE
12 1Canexis Pharma
13 4Catalent Pharma Solutions
14 1Chemport Inc
15 2Curia
16 1Gelita Health GmbH
17 1Jubilant HollisterStier
18 1Mallinckrodt Pharmaceuticals
19 1MediPharm Labs
20 1NATIONAL CENTER FOR NATURAL PRODUCTS RESEARCH
21 1National Institute on Drug Abuse
22 1Norac Pharma
23 1Resolution Chemicals Limited
24 1S AND B PHARMA INC DBA NORAC PHARMA
25 1Sichuan Gowell Pharmaceutical
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01 1Canada
02 2China
03 2Germany
04 1India
05 1Ireland
06 1Netherlands
07 1South Korea
08 1Switzerland
09 19U.S.A
10 2United Kingdom
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01 14Active
02 7Inactive
03 10Blank
01 2Valid
02 29Blank
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Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
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 : 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 Marinol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Marinol, including repackagers and relabelers. The FDA regulates Marinol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Marinol 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 Marinol supplier is an individual or a company that provides Marinol active pharmaceutical ingredient (API) or Marinol finished formulations upon request. The Marinol suppliers may include Marinol API manufacturers, exporters, distributors and traders.
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