01 1Hainan Poly Pharm
02 1TOPHARMAN SHANDONG CO LTD
01 2China
01 2Active
01 2Blank
01 2Blank
01 2Blank
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39308
Submission : 2024-01-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38852
Submission : 2023-09-20
Status : Active
Type : II
NDC Package Code : 14335-680
Start Marketing Date : 2023-09-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
A Tecovirimat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tecovirimat, including repackagers and relabelers. The FDA regulates Tecovirimat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tecovirimat API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Tecovirimat supplier is an individual or a company that provides Tecovirimat active pharmaceutical ingredient (API) or Tecovirimat finished formulations upon request. The Tecovirimat suppliers may include Tecovirimat API manufacturers, exporters, distributors and traders.
click here to find a list of Tecovirimat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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