Aztreonam - 63323-397-20 - (AZTREONAM)

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Drug Information of Aztreonam

Product NDC: 63323-397
Proprietary Name: Aztreonam
Non Proprietary Name: AZTREONAM
Active Ingredient(s): 500    mg/1 & nbsp;   AZTREONAM
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Aztreonam

Product NDC: 63323-397
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065439
Marketing Category: ANDA
Start Marketing Date: 20091105

Package Information of Aztreonam

Package NDC: 63323-397-20
Package Description: 10 VIAL in 1 TRAY (63323-397-20) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

NDC Information of Aztreonam

NDC Code 63323-397-20
Proprietary Name Aztreonam
Package Description 10 VIAL in 1 TRAY (63323-397-20) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Product NDC 63323-397
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AZTREONAM
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20091105
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name AZTREONAM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Monobactam Antibacterial [EPC],Monobactams [Chemical/Ingredient]

Complete Information of Aztreonam


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