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Nitrofurantoin - 0615-7655-39 - (Nitrofurantoin)

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Drug Information of Nitrofurantoin

Product NDC: 0615-7655
Proprietary Name: Nitrofurantoin
Non Proprietary Name: Nitrofurantoin
Active Ingredient(s): 100    mg/1 & nbsp;   Nitrofurantoin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nitrofurantoin

Product NDC: 0615-7655
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074967
Marketing Category: ANDA
Start Marketing Date: 20110506

Package Information of Nitrofurantoin

Package NDC: 0615-7655-39
Package Description: 30 CAPSULE in 1 BLISTER PACK (0615-7655-39)

NDC Information of Nitrofurantoin

NDC Code 0615-7655-39
Proprietary Name Nitrofurantoin
Package Description 30 CAPSULE in 1 BLISTER PACK (0615-7655-39)
Product NDC 0615-7655
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nitrofurantoin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110506
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name NITROFURANTOIN
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient]

Complete Information of Nitrofurantoin


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