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Imipenem and Cilastatin - 0409-3507-05 - (IMIPENEM and CILASTATIN SODIUM)

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Drug Information of Imipenem and Cilastatin

Product NDC: 0409-3507
Proprietary Name: Imipenem and Cilastatin
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 Imipenem and Cilastatin

Product NDC: 0409-3507
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090825
Marketing Category: ANDA
Start Marketing Date: 20111117

Package Information of Imipenem and Cilastatin

Package NDC: 0409-3507-05
Package Description: 10 BOTTLE in 1 CARTON (0409-3507-05) > 100 mL in 1 BOTTLE

NDC Information of Imipenem and Cilastatin

NDC Code 0409-3507-05
Proprietary Name Imipenem and Cilastatin
Package Description 10 BOTTLE in 1 CARTON (0409-3507-05) > 100 mL in 1 BOTTLE
Product NDC 0409-3507
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 20111117
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
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 Imipenem and Cilastatin


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