Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
01 1Vamsi Labs
02 1LGM Pharma
03 1Jai Radhe Sales
04 1Aarti Pharmalabs
05 1Neuland Laboratories
06 1Amphastar Pharmaceuticals
07 1Aspire Lifesciences Pvt Ltd
08 1Beijing Fukangren Biopharmaceutical
09 1Boehringer Ingelheim GmbH
10 1CR Double-Crane Pharmaceuticals Co., Ltd
11 1Cipla
12 1DEAFARMA
13 1Derivados Quimicos SAU
14 1Guangzhou Tosun Pharmaceutical
15 1Hunan Warrant Chiral Pharmaceutical
16 1Jayco Chemical Industries
17 1Lusochimica
18 1Melody Healthcare Pvt Ltd
19 1Olon S.p.A
20 1R L Fine Chem
21 1Resonance Laboratories Pvt. Ltd
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25 1Zenfold Sustainable Technologies
26 1Zhejiang Ausun Pharmaceutical
01 5China
02 1Germany
03 13India
04 4Italy
05 1Spain
06 2U.S.A
01 6Active
02 2Inactive
03 18Blank
01 7Valid
02 1Withdrawn by Holder
03 18Blank
01 1220MF10081
02 25Blank
01 1WC-0036
02 1WC-0099
03 1WC-0142
04 1WC-0155
05 1WC-0227
06 21Blank
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
Date of Issue : 2022-06-13
Valid Till : 2025-07-02
Written Confirmation Number : WC-0155
Address of the Firm :
NDC Package Code : 66412-0753
Start Marketing Date : 2019-09-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21179
Submission : 2007-12-15
Status : Active
Type : II
Certificate Number : R1-CEP 2008-150 - Rev 03
Issue Date : 2022-10-14
Type : Chemical
Substance Number : 919
Status : Valid
Date of Issue : 2023-01-06
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm :
NDC Package Code : 15308-1001
Start Marketing Date : 2002-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-01-15
Pay. Date : 2014-01-03
DMF Number : 15130
Submission : 2000-11-06
Status : Active
Type : II
Certificate Number : R1-CEP 2012-126 - Rev 02
Issue Date : 2023-04-14
Type : Chemical
Substance Number : 919
Status : Valid
Date of Issue : 2022-07-28
Valid Till : 2025-06-16
Written Confirmation Number : WC-0036
Address of the Firm :
NDC Package Code : 58032-0100
Start Marketing Date : 2015-04-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/1)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-07-02
Registration Number : 20130614-188-I-356-02(A)
Manufacturer Name : Neuland Laboratories Ltd.
Manufacturer Address : Unit-I, Sy. No: 347, 473, 474, 490/2, Bonthapally Village, Veerabhadraswamy Temple Road, Gummadidala Mandal, Sangareddy District - 502 313, Telangana State, India
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-02-05
Pay. Date : 2015-01-27
DMF Number : 8979
Submission : 1991-02-15
Status : Active
Type : II
Certificate Number : R1-CEP 2004-220 - Rev 01
Issue Date : 2020-11-26
Type : Chemical
Substance Number : 919
Status : Valid
NDC Package Code : 43898-0102
Start Marketing Date : 1991-02-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Takeda Pharmaceutical Company Korea Ltd.
Registration Date : 2013-10-20
Registration Number : 20131020-188-I-346-04
Manufacturer Name : Lusochimica SpA
Manufacturer Address : Lomagna (LC) - Via Giotto 9, Italy
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14259
Submission : 1999-06-25
Status : Active
Type : II
Certificate Number : R1-CEP 1996-005 - Rev 05
Issue Date : 2015-10-08
Type : Chemical
Substance Number : 919
Status : Valid
Registration Number : 220MF10081
Registrant's Address : Binger Strasse 173,55216 Ingelheim am Rhein
Initial Date of Registration : 2008-03-14
Latest Date of Registration : --
NDC Package Code : 12714-049
Start Marketing Date : 2011-05-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Boehringer Ingelheim Korea Ltd.
Registration Date : 2012-09-19
Registration Number : 20120919-188-I-64-01
Manufacturer Name : Boehringer Ingelheim Pharma GmbH & Co. K.G.
Manufacturer Address : Binger Strasse 173, 55216 Ingelheim am Rhein
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-02-17
Pay. Date : 2013-09-12
DMF Number : 8973
Submission : 1991-02-18
Status : Active
Type : II
Registrant Name : Hanlim Pharmaceutical Co., Ltd.
Registration Date : 2018-06-27
Registration Number : 20130806-188-I-301-03(2)
Manufacturer Name : Sifavitor Srl
Manufacturer Address : Casaletto Lodigiano (LO) - Via Livelli, 1 - Fraz. Mairano, Italy.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23135
Submission : 2009-09-28
Status : Inactive
Type : II
NDC Package Code : 59349-0013
Start Marketing Date : 2018-11-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29843
Submission : 2015-10-01
Status : Inactive
Type : II
Certificate Number : R0-CEP 2015-340 - Rev 00
Issue Date : 2016-12-16
Type : Chemical
Substance Number : 919
Status : Withdrawn by Holder
Date of Issue : 2022-06-17
Valid Till : 2025-08-04
Written Confirmation Number : WC-0142
Address of the Firm :
NDC Package Code : 53104-7704
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
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