01 1Abelei
02 1David Michael Co
03 3Fona International
04 2Kerry
05 1Robertet
06 1Symrise
07 1Takasago International
08 1Tastepoint by IFF
09 2Ungerer and Company
01 1188A10 NATURAL RASPBERRY TYPE FLAVOR
02 130632403 N&A RASPBERRY FL
03 1652742 RASPBERRY FLAVOR SD
04 1906.0088U N-C RASPBERRY FLAVOR, ART
05 1906.0207U N-C RASPBERRY FLAVOR, NAT & ART
06 1906.264 VERY RASPBERRY (AN ARTIFICIAL FLAVOR)
07 1ARTIFICIAL JUICY RASPBERRY FLAVOR FW-4870
08 1ARTIFICIAL RASPBERRY FLAVOR # 7557-A
09 1ARTIFICIAL RASPBERRY FLAVOR TAK-153945
10 1BLUE RASPBERRY NAT/ARTIFICIAL FLAVOR 707760
11 1MICHAELOK® NATURAL RASPBERRY FLAVOR WONF #4975
12 1NATURAL AND ARTIFICIAL RASPBERRY FLAVOR FZ 6963
13 1SPRAY DRIED ARTIFICIAL FLAVOR (CHERRY RASPBERRY TYPE) FOR ANTIBIOTIC NV-7759
01 1Germany
02 1Japan
03 11U.S.A
01 11Active
02 2Inactive
01 13Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30783
Submission : 2016-07-28
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29946
Submission : 2015-10-22
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32249
Submission : 2017-11-10
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21312
Submission : 2008-02-05
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15320
Submission : 2001-03-02
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28579
Submission : 2014-08-18
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15474
Submission : 2001-05-29
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30149
Submission : 2015-12-24
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22114
Submission : 2008-10-17
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27305
Submission : 2013-07-08
Status : Active
Type : IV
11
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A Tox21_202789 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202789, including repackagers and relabelers. The FDA regulates Tox21_202789 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202789 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 Tox21_202789 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_202789 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_202789 DMFs exist exist since differing nations have different regulations, such as Tox21_202789 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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