Folic Acid - 49349-358-02 - (Folic Acid)

Alphabetical Index


Drug Information of Folic Acid

Product NDC: 49349-358
Proprietary Name: Folic Acid
Non Proprietary Name: Folic Acid
Active Ingredient(s): 1    mg/1 & nbsp;   Folic Acid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Folic Acid

Product NDC: 49349-358
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040625
Marketing Category: ANDA
Start Marketing Date: 20110708

Package Information of Folic Acid

Package NDC: 49349-358-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-358-02)

NDC Information of Folic Acid

NDC Code 49349-358-02
Proprietary Name Folic Acid
Package Description 30 TABLET in 1 BLISTER PACK (49349-358-02)
Product NDC 49349-358
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Folic Acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110708
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name FOLIC ACID
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Folic Acid


General Information