Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
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01 1Tenatra Chemie
02 1HUNAN JIUDIAN PHARMACEUTICAL CO LTD
03 1INTERNATIONAL SPECIALTY PRODUCTS
04 1ISP Sutton Laboratories
05 1PharmHe Global Corp
06 1Salicylates and Chemicals
07 1Spectrum Chemical
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01 2China
02 2India
03 3U.S.A
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01 1Active
02 6Blank
01 7Blank
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01 7Blank
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01 7Blank
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01 7Blank
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01 149452-0260
02 149574-516
03 151040-000
04 176107-900
05 3Blank
01 7Blank
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15310
Submission : 2001-02-21
Status : Active
Type : II
NDC Package Code : 49574-516
Start Marketing Date : 2017-05-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76107-900
Start Marketing Date : 2012-11-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51040-000
Start Marketing Date : 2012-06-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-0260
Start Marketing Date : 2009-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Glyoxyldiureide 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 Glyoxyldiureide manufacturer or Glyoxyldiureide supplier for your needs.
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A Allantoin, European Pharmacopoeia (EP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Allantoin, European Pharmacopoeia (EP) Reference Standard, including repackagers and relabelers. The FDA regulates Allantoin, European Pharmacopoeia (EP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Allantoin, European Pharmacopoeia (EP) Reference Standard 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 Allantoin, European Pharmacopoeia (EP) Reference Standard supplier is an individual or a company that provides Allantoin, European Pharmacopoeia (EP) Reference Standard active pharmaceutical ingredient (API) or Allantoin, European Pharmacopoeia (EP) Reference Standard finished formulations upon request. The Allantoin, European Pharmacopoeia (EP) Reference Standard suppliers may include Allantoin, European Pharmacopoeia (EP) Reference Standard API manufacturers, exporters, distributors and traders.
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We have 7 companies offering Allantoin, European Pharmacopoeia (EP) Reference Standard
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