Nafcillin - 55150-122-15 - (Nafcillin Sodium)

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Drug Information of Nafcillin

Product NDC: 55150-122
Proprietary Name: Nafcillin
Non Proprietary Name: Nafcillin Sodium
Active Ingredient(s): 1    g/4mL & nbsp;   Nafcillin Sodium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nafcillin

Product NDC: 55150-122
Labeler Name: AuroMedics Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091613
Marketing Category: ANDA
Start Marketing Date: 20121226

Package Information of Nafcillin

Package NDC: 55150-122-15
Package Description: 10 VIAL in 1 BOX (55150-122-15) > 4 mL in 1 VIAL

NDC Information of Nafcillin

NDC Code 55150-122-15
Proprietary Name Nafcillin
Package Description 10 VIAL in 1 BOX (55150-122-15) > 4 mL in 1 VIAL
Product NDC 55150-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nafcillin Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20121226
Marketing Category Name ANDA
Labeler Name AuroMedics Pharma LLC
Substance Name NAFCILLIN SODIUM
Strength Number 1
Strength Unit g/4mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Nafcillin


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