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

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03 1Jai Radhe Sales
04 3Willow Birch Pharma
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01 1221MF10281
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01 120250221-211-J-1776
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01 310695-052
02 138779-2468
03 149885-0006
04 151927-5152
05 155018-121
06 155018-221
07 158623-0047
08 160592-316
09 162991-3195
10 166405-0001
11 168171-0001
12 171052-225
13 173212-079
14 173377-144
15 177382-0060
16 177382-0100
17 177382-0110
18 185411-118
19 185512-2053
20 185512-3053
21 285614-201
22 185694-004
23 185941-008
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01 15476
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03 15576
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
NDC Package Code : 10695-052
Start Marketing Date : 2019-09-23
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
NDC Package Code : 10695-052
Start Marketing Date : 2019-03-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
NDC Package Code : 10695-052
Start Marketing Date : 2019-03-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-09
Pay. Date : 2012-12-14
DMF Number : 21395
Submission : 2008-03-05
Status : Active
Type : II
Certificate Number : R1-CEP 1998-138 - Rev 05
Issue Date : 2020-02-28
Type : Chemical
Substance Number : 1336
Status : Valid
Registration Number : 221MF10281
Registrant's Address : Estrada Coronel Nicolau de Mesquita Taipa, Macau S. A. R. China
Initial Date of Registration : 2009-12-18
Latest Date of Registration :
NDC Package Code : 55018-221
Start Marketing Date : 2009-03-19
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : Reviewed
Rev. Date : 2022-04-06
Pay. Date : 2022-01-13
DMF Number : 36494
Submission : 2021-11-15
Status : Active
Type : II

GDUFA
DMF Review : Reviewed
Rev. Date : 2014-02-08
Pay. Date : 2012-12-18
DMF Number : 21624
Submission : 2008-05-08
Status : Active
Type : II
Certificate Number : CEP 2025-175 - Rev 01
Issue Date : 2025-11-17
Type : Chemical
Substance Number : 1336
Status : Valid
Registration Number : 304MF10048
Registrant's Address : 46 Waisha Road, Jiaojiang District, Taizhou City, Zhejiang Province, P. R. China 318000
Initial Date of Registration : 2022-03-02
Latest Date of Registration :
NDC Package Code : 58623-0047
Start Marketing Date : 2014-10-24
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2025-02-21
Registration Number : 20250221-211-J-1776
Manufacturer Name : Zhejiang Hisun Pharmaceutical Co., Ltd.
Manufacturer Address : 56 Binhai Road, Jiaojiang District, Taizhou City, Zhejiang Province, People's Republic of China
VMF Number : 5553
Submission : 1995-12-14
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17673
Submission : 2004-07-18
Status : Inactive
Type : II

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PharmaCompass offers a list of Ivermectin 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 Ivermectin manufacturer or Ivermectin supplier for your needs.
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A Stromectol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stromectol, including repackagers and relabelers. The FDA regulates Stromectol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stromectol 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 Stromectol supplier is an individual or a company that provides Stromectol active pharmaceutical ingredient (API) or Stromectol finished formulations upon request. The Stromectol suppliers may include Stromectol API manufacturers, exporters, distributors and traders.
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We have 40 companies offering Stromectol
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