01 3Bristol Myers Squibb
02 1Fresenius Kabi AB Brunna
01 1Sweden
02 3U.S.A
01 1Active
02 3Inactive
01 4Blank
01 4Blank
01 4Blank
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26189
Submission : 2012-06-29
Status : Active
Type : II
NDC Package Code : 66558-0206
Start Marketing Date : 2011-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13428
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13430
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14213
Submission : 1990-04-05
Status : Inactive
Type : II
A Hetacillin Potassium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hetacillin Potassium, including repackagers and relabelers. The FDA regulates Hetacillin Potassium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hetacillin Potassium 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 Hetacillin Potassium supplier is an individual or a company that provides Hetacillin Potassium active pharmaceutical ingredient (API) or Hetacillin Potassium finished formulations upon request. The Hetacillin Potassium suppliers may include Hetacillin Potassium API manufacturers, exporters, distributors and traders.
click here to find a list of Hetacillin Potassium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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