LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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01 1LGM Pharma
02 1Jai Radhe Sales
03 1HRV Pharma
04 1Tenatra Exports
05 2Swati Spentose
06 1Aura Pharmaceuticals
07 1Biopeptek Pharmaceuticals
08 1Cadila Pharmaceuticals
09 1Changzhou Yabang- QH Pharmachem Co
10 1Cipla
11 1Delmar Biopharma
12 1Evereen Shanghai Biotechnology
13 1Formil Quimica Ltd
14 1Guilin Pharmaceutical Ltd
15 1Hebei Veyong Pharmaceutical
16 2Johnson & Johnson Innovative Medicine
17 1Letco Medical
18 1Lohitha Lifesciences
19 2MSN Laboratories
20 1Optimus Pharma
21 1Parth Antibiotics
22 1Pcca
23 1Progress Life Sciences
24 1Sekhmet Pharmaventures
25 1Shaanxi Hanjiang pharmaceutical Group Co
26 1Solara Active Pharma Sciences
27 1Willow Birch Pharma
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03 17India
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01 112578-618
02 151927-0336
03 153104-7510
04 159285-011
05 160592-247
06 162991-1544
07 169766-038
08 171052-168
09 172643-035
10 173212-103
11 173377-260
12 182891-028
13 185512-2115
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
SWATI – Transforming science into solutions with 50+ years of expertise, global accreditations, and pioneering biotech innovation.
SWATI – Transforming science into solutions with 50+ years of expertise, global accreditations, and pioneering biotech innovation.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30325
Submission : 2016-03-28
Status : Active
Type : II
Certificate Number : R1-CEP 1999-020 - Rev 06
Issue Date : 2022-10-27
Type : Chemical
Substance Number : 845
Status : Valid

GDUFA
DMF Review : Reviewed
Rev. Date : 2017-10-05
Pay. Date : 2017-09-05
DMF Number : 32016
Submission : 2017-09-07
Status : Active
Type : II
NDC Package Code : 59285-011
Start Marketing Date : 2017-10-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : Reviewed
Rev. Date : 2021-06-16
Pay. Date : 2021-05-27
DMF Number : 35415
Submission : 2020-12-28
Status : Active
Type : II
NDC Package Code : 72643-035
Start Marketing Date : 2023-06-30
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7804
Submission : 1988-12-06
Status : Inactive
Type : II

17
PharmaCompass offers a list of Mebendazole 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 Mebendazole manufacturer or Mebendazole supplier for your needs.
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A Mebutar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mebutar, including repackagers and relabelers. The FDA regulates Mebutar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mebutar 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 Mebutar supplier is an individual or a company that provides Mebutar active pharmaceutical ingredient (API) or Mebutar finished formulations upon request. The Mebutar suppliers may include Mebutar API manufacturers, exporters, distributors and traders.
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We have 27 companies offering Mebutar
Get in contact with the supplier of your choice: