Folic Acid - 49349-723-30 - (Folic Acid)

Alphabetical Index


Drug Information of Folic Acid

Product NDC: 49349-723
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: 49349-723
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040796
Marketing Category: ANDA
Start Marketing Date: 20130228

Package Information of Folic Acid

Package NDC: 49349-723-30
Package Description: 400 TABLET in 1 CANISTER (49349-723-30)

NDC Information of Folic Acid

NDC Code 49349-723-30
Proprietary Name Folic Acid
Package Description 400 TABLET in 1 CANISTER (49349-723-30)
Product NDC 49349-723
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Folic Acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130228
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