Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.

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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32240
Submission : 2018-08-30
Status : Active
Type : II
NDC Package Code : 55570-520
Start Marketing Date : 2013-12-10
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 : 34040
Submission : 2019-09-16
Status : Active
Type : II
Certificate Number : CEP 2018-254 - Rev 02
Issue Date : 2025-01-29
Type : Chemical
Substance Number : 252
Status : Valid
NDC Package Code : 72955-318
Start Marketing Date : 2025-10-22
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (97kg/97kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26398
Submission : 2012-09-07
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23634
Submission : 2010-05-06
Status : Inactive
Type : II


Certificate Number : R1-CEP 2017-015 - Rev 00
Issue Date : 2023-07-31
Type : Chemical
Substance Number : 252
Status : Valid
NDC Package Code : 80723-100
Start Marketing Date : 2020-10-07
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING



Certificate Number : R1-CEP 2012-347 - Rev 01
Issue Date : 2022-04-13
Type : Chemical
Substance Number : 252
Status : Valid
NDC Package Code : 80723-400
Start Marketing Date : 2022-10-27
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING

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PharmaCompass offers a list of Zinc Oxide 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 Zinc Oxide manufacturer or Zinc Oxide supplier for your needs.
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A CI 77947 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CI 77947, including repackagers and relabelers. The FDA regulates CI 77947 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CI 77947 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 CI 77947 supplier is an individual or a company that provides CI 77947 active pharmaceutical ingredient (API) or CI 77947 finished formulations upon request. The CI 77947 suppliers may include CI 77947 API manufacturers, exporters, distributors and traders.
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We have 40 companies offering CI 77947
Get in contact with the supplier of your choice: