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Nitrofurantoin (macrocrystals) - 55289-186-21 - (nitrofurantoin (macrocrystals))

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Drug Information of Nitrofurantoin (macrocrystals)

Product NDC: 55289-186
Proprietary Name: Nitrofurantoin (macrocrystals)
Non Proprietary Name: nitrofurantoin (macrocrystals)
Active Ingredient(s): 50    mg/1 & nbsp;   nitrofurantoin (macrocrystals)
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nitrofurantoin (macrocrystals)

Product NDC: 55289-186
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074967
Marketing Category: ANDA
Start Marketing Date: 20110506

Package Information of Nitrofurantoin (macrocrystals)

Package NDC: 55289-186-21
Package Description: 21 CAPSULE in 1 BOTTLE, PLASTIC (55289-186-21)

NDC Information of Nitrofurantoin (macrocrystals)

NDC Code 55289-186-21
Proprietary Name Nitrofurantoin (macrocrystals)
Package Description 21 CAPSULE in 1 BOTTLE, PLASTIC (55289-186-21)
Product NDC 55289-186
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nitrofurantoin (macrocrystals)
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110506
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name NITROFURANTOIN
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient]

Complete Information of Nitrofurantoin (macrocrystals)


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