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Nitrofurantoin Monohydrate/Macrocrystals - 54868-6203-2 - (Nitrofurantoin Monohydrate and Nitrofurantoin, macrocrystalline)

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Drug Information of Nitrofurantoin Monohydrate/Macrocrystals

Product NDC: 54868-6203
Proprietary Name: Nitrofurantoin Monohydrate/Macrocrystals
Non Proprietary Name: Nitrofurantoin Monohydrate and Nitrofurantoin, macrocrystalline
Active Ingredient(s): 25; 75    mg/1; mg/1 & nbsp;   Nitrofurantoin Monohydrate and Nitrofurantoin, macrocrystalline
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nitrofurantoin Monohydrate/Macrocrystals

Product NDC: 54868-6203
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076648
Marketing Category: ANDA
Start Marketing Date: 20110106

Package Information of Nitrofurantoin Monohydrate/Macrocrystals

Package NDC: 54868-6203-2
Package Description: 6 CAPSULE in 1 BOTTLE, PLASTIC (54868-6203-2)

NDC Information of Nitrofurantoin Monohydrate/Macrocrystals

NDC Code 54868-6203-2
Proprietary Name Nitrofurantoin Monohydrate/Macrocrystals
Package Description 6 CAPSULE in 1 BOTTLE, PLASTIC (54868-6203-2)
Product NDC 54868-6203
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nitrofurantoin Monohydrate and Nitrofurantoin, macrocrystalline
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110106
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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