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Nitrofurantoin - 49349-040-04 - (Nitrofurantoin)

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Drug Information of Nitrofurantoin

Product NDC: 49349-040
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: 49349-040
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073652
Marketing Category: ANDA
Start Marketing Date: 20111110

Package Information of Nitrofurantoin

Package NDC: 49349-040-04
Package Description: 14 CAPSULE in 1 BLISTER PACK (49349-040-04)

NDC Information of Nitrofurantoin

NDC Code 49349-040-04
Proprietary Name Nitrofurantoin
Package Description 14 CAPSULE in 1 BLISTER PACK (49349-040-04)
Product NDC 49349-040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nitrofurantoin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20111110
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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