Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Laboratorium Ofichem B.V
02 1Anmol Chemicals
03 1Dr. Paul Lohmann GmbH KG
04 1Fuji Chemical Industry
05 1Global Calcium
06 1Jost Chemical
07 1Purity Chemicals
08 1Quality Chemicals
09 1Sudeep Pharma
10 1Valaji PharmaChem
11 1Vasa Pharmachem
12 1Vertellus
13 1West Bengal Chemicals Industries
01 1Germany
02 6India
03 1Japan
04 1Netherlands
05 2Spain
06 2U.S.A
01 1Active
02 12Blank
01 1Valid
02 12Blank
01 1304MF10017
02 1304MF10096
03 1304MF10105
04 1306MF10011
05 9Blank
01 1WC-0104A5-A6
02 1WC-0518
03 11Blank
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Registration Number : 304MF10017
Registrant's Address : Heembadweg 5, 9561 CZ Ter apel, The Netherlands
Initial Date of Registration : 2022-01-20
Latest Date of Registration : --
NDC Package Code : 62675-1444
Start Marketing Date : 2018-07-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF |
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36872
Submission : 2022-04-18
Status : Active
Type : II
Date of Issue : 2022-06-07
Valid Till : 2022-07-07
Written Confirmation Number : WC-0104A5-A6
Address of the Firm :
NDC Package Code : 64162-0219
Start Marketing Date : 2023-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Registration Number : 306MF10011
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2024-01-17
Latest Date of Registration : --
Certificate Number : R0-CEP 2018-117 - Rev 01
Issue Date : 2023-02-02
Type : Chemical
Substance Number : 1482
Status : Valid
A Zinc Acetate Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinc Acetate Dihydrate, including repackagers and relabelers. The FDA regulates Zinc Acetate Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinc Acetate Dihydrate 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 Zinc Acetate Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zinc Acetate Dihydrate supplier is an individual or a company that provides Zinc Acetate Dihydrate active pharmaceutical ingredient (API) or Zinc Acetate Dihydrate finished formulations upon request. The Zinc Acetate Dihydrate suppliers may include Zinc Acetate Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Zinc Acetate Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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