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NITROFURANTOIN - 49349-021-02 - (NITROFURANTOIN)

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Drug Information of NITROFURANTOIN

Product NDC: 49349-021
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: 49349-021
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077025
Marketing Category: ANDA
Start Marketing Date: 20100917

Package Information of NITROFURANTOIN

Package NDC: 49349-021-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-021-02)

NDC Information of NITROFURANTOIN

NDC Code 49349-021-02
Proprietary Name NITROFURANTOIN
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-021-02)
Product NDC 49349-021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NITROFURANTOIN
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100917
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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