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Nitrofurantoin (monohydrate/macrocrystals) - 0185-0122-10 - (Nitrofurantoin (monohydrate/macrocrystals))

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Drug Information of Nitrofurantoin (monohydrate/macrocrystals)

Product NDC: 0185-0122
Proprietary Name: Nitrofurantoin (monohydrate/macrocrystals)
Non Proprietary Name: Nitrofurantoin (monohydrate/macrocrystals)
Active Ingredient(s): 25; 75    mg/1; mg/1 & nbsp;   Nitrofurantoin (monohydrate/macrocrystals)
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nitrofurantoin (monohydrate/macrocrystals)

Product NDC: 0185-0122
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080043
Marketing Category: ANDA
Start Marketing Date: 19701125

Package Information of Nitrofurantoin (monohydrate/macrocrystals)

Package NDC: 0185-0122-10
Package Description: 1000 CAPSULE in 1 BOTTLE (0185-0122-10)

NDC Information of Nitrofurantoin (monohydrate/macrocrystals)

NDC Code 0185-0122-10
Proprietary Name Nitrofurantoin (monohydrate/macrocrystals)
Package Description 1000 CAPSULE in 1 BOTTLE (0185-0122-10)
Product NDC 0185-0122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nitrofurantoin (monohydrate/macrocrystals)
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19701125
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE
Strength Number 25; 75
Strength Unit mg/1; mg/1
Pharmaceutical Classes Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient],Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient]

Complete Information of Nitrofurantoin (monohydrate/macrocrystals)


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