01 1GSK
02 1UQUIFA
03 1ZOETIS
01 1Spain
02 1U.S.A
03 1United Kingdom
01 3Blank
01 3Blank
01 3Blank
01 3Blank
01 3Blank
01 152286-0003
02 2Blank
01 15361
02 15466
03 1Blank
VMF Number : 5466
Submission : 1993-09-07
Status : Active
Type : II
VMF Number : 5361
Submission : 1991-06-21
Status : Inactive
Type : II
NDC Package Code : 52286-0003
Start Marketing Date : 2009-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A DSSTox_CID_31392 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_31392, including repackagers and relabelers. The FDA regulates DSSTox_CID_31392 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_31392 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 DSSTox_CID_31392 supplier is an individual or a company that provides DSSTox_CID_31392 active pharmaceutical ingredient (API) or DSSTox_CID_31392 finished formulations upon request. The DSSTox_CID_31392 suppliers may include DSSTox_CID_31392 API manufacturers, exporters, distributors and traders.
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