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Nitrofurantoin (macrocrystals) - 51079-584-20 - (Nitrofurantoin (macrocrystals))

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Drug Information of Nitrofurantoin (macrocrystals)

Product NDC: 51079-584
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: 51079-584
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074967
Marketing Category: ANDA
Start Marketing Date: 20110114

Package Information of Nitrofurantoin (macrocrystals)

Package NDC: 51079-584-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-584-20) > 1 CAPSULE in 1 BLISTER PACK (51079-584-01)

NDC Information of Nitrofurantoin (macrocrystals)

NDC Code 51079-584-20
Proprietary Name Nitrofurantoin (macrocrystals)
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-584-20) > 1 CAPSULE in 1 BLISTER PACK (51079-584-01)
Product NDC 51079-584
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nitrofurantoin (macrocrystals)
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110114
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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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