Rampex Labs – Simplifying Synthesis with Innovation, Quality, and Commitment to Global Pharmaceutical Excellence.

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01 17Active
02 3Inactive
03 41Blank
01 2Expired
02 16Valid
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01 1219MF10022
02 1219MF10374
03 1221MF10130
04 1302MF10019
05 1306MF10103
06 1307MF10012
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01 2WC-0043
02 1WC-0074
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01 120050831-47-B-122-04
02 120050831-47-B-122-04(1)
03 120070302-47-B-256-10
04 120081031-47-B-284-12
05 120081031-47-B-284-12(1)
06 120100226-47-B-298-13(1)
07 120120925-47-B-347-16
08 120120925-47-B-347-16(2)
09 120120925-47-B-347-16(3)
10 120120925-47-B-347-16(4)
11 120130313-47-B-343-17
12 120210426-47-B-440-20
13 120210426-47-B-440-20(1)
14 120250624-47-B-491-22
15 47Blank
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01 138779-2415
02 151846-1025
03 151927-0075
04 151927-4320
05 153104-7540
06 155111-017
07 157451-1153
08 159116-1850
09 159116-1851
10 159116-1852
11 159116-1853
12 162756-109
13 162991-2599
14 163850-2706
15 164567-0005
16 165129-2161
17 165691-0035
18 165862-377
19 166022-0204
20 166651-903
21 167835-5014
22 169056-009
23 173377-244
24 184671-1025
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Rampex Labs – Simplifying Synthesis with Innovation, Quality, and Commitment to Global Pharmaceutical Excellence.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16317
Submission : 2002-12-13
Status : Active
Type : II
Certificate Number : R1-CEP 2005-056 - Rev 00
Issue Date : 2012-05-24
Type : Chemical
Substance Number : 2016
Status : Valid
NDC Package Code : 64567-0005
Start Marketing Date : 2009-08-19
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-09-23
Pay. Date : 2015-09-09
DMF Number : 15436
Submission : 2001-05-15
Status : Active
Type : II
Certificate Number : R1-CEP 2005-071 - Rev 06
Issue Date : 2023-05-23
Type : Chemical
Substance Number : 2016
Status : Valid
Registration Number : 302MF10019
Registrant's Address : 8-2-337, Road No. 3,Banjara Hills,Hyderabad 500 034,TELANGANA,INDIA
Initial Date of Registration : 2020-01-31
Latest Date of Registration :
Date of Issue : 2025-07-25
Valid Till : 2028-06-04
Written Confirmation Number : WC-0043
Address of the Firm :
NDC Package Code : 55111-017
Start Marketing Date : 2010-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Sangjin Trading Co., Ltd.
Registration Date : 2021-06-22
Registration Number : 20210426-47-B-440-20(1)
Manufacturer Name : Dr. Reddy's Laboratories Ltd.
Manufacturer Address : Peddadevulapally Village, Tripuraram Mandal, Nalgonda District - 508 207, Telangana State, India
| Available Reg Filing : CDMF |
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15642
Submission : 2001-10-01
Status : Active
Type : II
Registration Number : 307MF10012
Registrant's Address : 13 Pallagi u(´)t, Debrecen, 4042-Hungary
Initial Date of Registration : 2025-01-09
Latest Date of Registration :
NDC Package Code : 84671-1025
Start Marketing Date : 2017-11-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF |
Delivering Quality APIs, Drug Intermediates, and Specialty Chemicals to Over 50 Countries Across the Globe.
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PharmaCompass offers a list of Ondansetron Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ondansetron Hydrochloride manufacturer or Ondansetron Hydrochloride supplier for your needs.
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A Emetron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emetron, including repackagers and relabelers. The FDA regulates Emetron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emetron 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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We have 47 companies offering Emetron
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