Emay Pharmaceuticals is a GMP-certified API manufacturing company.

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01 1Emay Pharmaceuticals
02 1Jai Radhe Sales
03 1Pharm-RX Chemical
04 1Supriya Lifescience
05 1Tenatra Exports
06 1Harika Drugs
07 1Ax Pharmaceutical Corporation
08 1Biesterfeld Spezialchemie GmbH
09 1Dr. Raju’s Pharma Solutions
10 1Green Waves
11 1Keshava Organics
12 1Kongo Chemical Co., Ltd.
13 1Merck & Co
14 1Oceanic Laboratories
15 1Sandoz B2B
16 1Spectrum Chemical
17 1Suvan Lifesciences
18 1Zeal Medipharma
19 1Zentiva
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01 1Canada
02 1Czech Republic
03 1Germany
04 10India
05 1Japan
06 1Switzerland
07 4U.S.A
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01 3Active
02 2Inactive
03 14Blank
01 1Valid
02 18Blank
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01 19Blank
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01 1WC-0133
02 1WC-0179n
03 1WC-0218
04 1WC-0244
05 15Blank
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01 19Blank
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01 112294-9994
02 149452-5171
03 161281-5000
04 166620-200
05 173377-023
06 14Blank
01 19Blank
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23512
Submission : 2010-01-22
Status : Active
Type : II
Certificate Number : CEP 2015-030 - Rev 01
Issue Date : 2025-04-02
Type : Chemical
Substance Number : 1357
Status : Valid
Date of Issue : 2025-09-02
Valid Till : 2028-07-02
Written Confirmation Number : WC-0218
Address of the Firm :
NDC Package Code : 61281-5000
Start Marketing Date : 2013-11-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF, CN |
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-06-19
Pay. Date : 2013-06-07
DMF Number : 8960
Submission : 1991-02-04
Status : Active
Type : II
NDC Package Code : 12294-9994
Start Marketing Date : 1972-06-29
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 : 35509
Submission : 2022-05-24
Status : Active
Type : II
Date of Issue : 2022-12-09
Valid Till : 2025-07-02
Written Confirmation Number : WC-0244
Address of the Firm :

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5733
Submission : 1985-02-26
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8538
Submission : 1990-04-26
Status : Inactive
Type : II

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A Avil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Avil, including repackagers and relabelers. The FDA regulates Avil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Avil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Avil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Avil supplier is an individual or a company that provides Avil active pharmaceutical ingredient (API) or Avil finished formulations upon request. The Avil suppliers may include Avil API manufacturers, exporters, distributors and traders.
click here to find a list of Avil suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
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