Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 1Nuray Chemicals Private Limited
03 1HRV Global Life Sciences
04 1Aurobindo Pharma Limited
05 1Steroid SpA
06 1Taro Pharmaceutical Industries
01 4India
02 1Italy
03 1U.S.A
01 4Active
02 1Inactive
03 1Blank
01 6Blank
01 6Blank
01 1WC-0416
02 1WC-0511
03 4Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-11-01
Pay. Date : 2020-09-24
DMF Number : 35203
Submission : 2020-09-12
Status : Active
Type : II
Date of Issue : 2021-10-22
Valid Till : 2024-10-21
Written Confirmation Number : WC-0511
Address of the Firm :
NDC Package Code : 73435-011
Start Marketing Date : 2020-12-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-02-25
Pay. Date : 2019-12-02
DMF Number : 34371
Submission : 2019-12-10
Status : Active
Type : II
Date of Issue : 2024-02-20
Valid Till : 2026-12-06
Written Confirmation Number : WC-0416
Address of the Firm :
NDC Package Code : 58159-071
Start Marketing Date : 2020-01-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26664
Submission : 2013-03-11
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-06-29
Pay. Date : 2018-06-12
DMF Number : 32861
Submission : 2018-06-12
Status : Active
Type : II
NDC Package Code : 59651-223
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3264
Submission : 1978-07-14
Status : Inactive
Type : II
A Diclofenamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diclofenamide, including repackagers and relabelers. The FDA regulates Diclofenamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diclofenamide 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 Diclofenamide supplier is an individual or a company that provides Diclofenamide active pharmaceutical ingredient (API) or Diclofenamide finished formulations upon request. The Diclofenamide suppliers may include Diclofenamide API manufacturers, exporters, distributors and traders.
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