PRIMAXIN - 0006-3552-59 - (imipenem and cilastatin sodium)

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Drug Information of PRIMAXIN

Product NDC: 0006-3552
Proprietary Name: PRIMAXIN
Non Proprietary Name: imipenem and cilastatin sodium
Active Ingredient(s): 500; 500    mg/100mL; mg/100mL & nbsp;   imipenem and cilastatin sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of PRIMAXIN

Product NDC: 0006-3552
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062756
Marketing Category: ANDA
Start Marketing Date: 19870108

Package Information of PRIMAXIN

Package NDC: 0006-3552-59
Package Description: 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0006-3552-59) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE

NDC Information of PRIMAXIN

NDC Code 0006-3552-59
Proprietary Name PRIMAXIN
Package Description 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0006-3552-59) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
Product NDC 0006-3552
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name imipenem and cilastatin sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19870108
Marketing Category Name ANDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name CILASTATIN SODIUM; IMIPENEM
Strength Number 500; 500
Strength Unit mg/100mL; mg/100mL
Pharmaceutical Classes Carbapenems [Chemical/Ingredient],Penem Antibacterial [EPC],Dipeptidase Inhibitors [MoA],Renal Dehydropeptidase Inhibitor [EPC]

Complete Information of PRIMAXIN


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