IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
01 1Inabata France S.A.S
02 1Suanfarma
03 1Laboratorium Ofichem B.V
04 1Alivira Animal Health
05 1Changzhou Yabang- QH Pharmachem Co
06 1Hebei Veyong Pharmaceutical
07 1Hubei Aoks Bio-tech
08 3Johnson & Johnson Innovative Medicine
09 1Nanjing Pharmaceutical
10 1Shaanxi Hanjiang pharmaceutical Group Co
11 1Tianhe Pharmaceutical
12 1Xian Tian Guangyuan Biotech
01 7China
02 1France
03 1India
04 1Netherlands
05 1Spain
06 3U.S.A
01 3Inactive
02 11Blank
01 3Valid
02 1Withdrawn by Holder
03 10Blank
01 14Blank
01 14Blank
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6079
Submission : 1985-10-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10995
Submission : 1994-07-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11015
Submission : 1994-08-02
Status : Inactive
Type : II
Certificate Number : CEP 2022-376 - Rev 00
Issue Date : 2024-04-16
Type : Chemical
Substance Number : 726
Status : Valid
Certificate Number : CEP 2022-498 - Rev 00
Issue Date : 2024-03-26
Type : Chemical
Substance Number : 726
Status : Valid
NDC Package Code : 69169-119
Start Marketing Date : 2021-08-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 6447
Submission : 2021-11-04
Status : Active
Type : II
Certificate Number : R1-CEP 1998-095 - Rev 01
Issue Date : 2009-09-18
Type : Chemical
Substance Number : 726
Status : Withdrawn by Holder
VMF Number : 5575
Submission : 1996-10-25
Status : Inactive
Type : II
Certificate Number : R1-CEP 2013-154 - Rev 01
Issue Date : 2022-06-23
Type : Chemical
Substance Number : 726
Status : Valid
A Levamisole Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levamisole Hydrochloride, including repackagers and relabelers. The FDA regulates Levamisole Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levamisole 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.
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A Levamisole Hydrochloride supplier is an individual or a company that provides Levamisole Hydrochloride active pharmaceutical ingredient (API) or Levamisole Hydrochloride finished formulations upon request. The Levamisole Hydrochloride suppliers may include Levamisole Hydrochloride API manufacturers, exporters, distributors and traders.
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