Deccan Nutraceuticals: A global leader in the integrated development, manufacturing, and marketing of pharmaceutical products.
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01 1Deccan Nutraceuticals Pvt. Ltd
02 1LGM Pharma
03 1HRV Global Life Sciences
04 1Tenatra Chemie
05 1Aurobindo Pharma Limited
06 1Beijing Fukangren Biopharmaceutical
07 1Biotechnica DWC
08 1Emcure Pharmaceuticals
09 2Enaltec Labs Private Limited
10 1F. Hoffmann-La Roche
11 1GLAND PHARMA LIMITED
12 1Harman Finochem
13 1Hetero Drugs
14 1Hubei Haosun Pharmaceutical Co., Ltd.
15 1Indoco Remedies Limited
16 2MSN Laboratories
17 1Mac-Chem Products (India) Pvt.Ltd
18 2Patheon
19 1Raks Pharma
20 1Royal DSM
21 1Surajlok Chemicals
22 2Tokyo Chemical Industry
23 1Varion Lifesciences
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01 1Algeria
02 2China
03 17India
04 2Japan
05 1Netherlands
06 1Switzerland
07 3U.S.A
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01 9Active
02 1Inactive
03 17Blank
01 6Valid
02 21Blank
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01 1217MF11158
02 1217MF11160
03 25Blank
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01 1WC-0017
02 1WC-0021
03 1WC-0021n
04 1WC-0045nA2
05 1WC-0152
06 1WC-0226
07 1WC-0275
08 1WC-0424
09 1WC-0424A4
10 1WC-0427A3-4
11 1WC-0435
12 16Blank
Deccan Nutraceuticals: A global leader in the integrated development, manufacturing, and marketing of pharmaceutical products.
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.
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-01-05
Pay. Date : 2016-11-07
DMF Number : 31003
Submission : 2016-11-30
Status : Active
Type : II
Date of Issue : 2019-07-15
Valid Till : 2022-07-15
Written Confirmation Number : WC-0152
Address of the Firm :
NDC Package Code : 14445-015
Start Marketing Date : 2016-11-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38087
Submission : 2023-02-24
Status : Active
Type : II
NDC Package Code : 14778-0707
Start Marketing Date : 2023-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-06-29
Pay. Date : 2015-04-29
DMF Number : 29197
Submission : 2015-03-31
Status : Active
Type : II
Certificate Number : R1-CEP 2016-044 - Rev 00
Issue Date : 2022-09-09
Type : Chemical
Substance Number : 626
Status : Valid
Date of Issue : 2022-06-17
Valid Till : 2025-07-14
Written Confirmation Number : WC-0021n
Address of the Firm :
NDC Package Code : 14501-0022
Start Marketing Date : 2015-04-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-02-14
Pay. Date : 2016-09-23
DMF Number : 30136
Submission : 2015-12-31
Status : Active
Type : II
Certificate Number : R0-CEP 2019-122 - Rev 01
Issue Date : 2021-01-08
Type : Chemical
Substance Number : 626
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-07-21
Written Confirmation Number : WC-0045nA2
Address of the Firm :
NDC Package Code : 66064-1020
Start Marketing Date : 2015-09-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-05-26
Pay. Date : 2014-05-14
DMF Number : 24760
Submission : 2011-03-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6941
Submission : 1987-04-20
Status : Inactive
Type : II
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PharmaCompass offers a list of Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate manufacturer or Neostigmine Methyl Sulfate supplier for your needs.
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A Neostigmine Methylsulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neostigmine Methylsulfate, including repackagers and relabelers. The FDA regulates Neostigmine Methylsulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neostigmine Methylsulfate 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 Neostigmine Methylsulfate supplier is an individual or a company that provides Neostigmine Methylsulfate active pharmaceutical ingredient (API) or Neostigmine Methylsulfate finished formulations upon request. The Neostigmine Methylsulfate suppliers may include Neostigmine Methylsulfate API manufacturers, exporters, distributors and traders.
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We have 23 companies offering Neostigmine Methylsulfate
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