Folic Acid - 63739-110-01 - (Folic Acid)

Alphabetical Index


Drug Information of Folic Acid

Product NDC: 63739-110
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: 63739-110
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080600
Marketing Category: ANDA
Start Marketing Date: 20041124

Package Information of Folic Acid

Package NDC: 63739-110-01
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-110-01) > 30 TABLET in 1 BLISTER PACK

NDC Information of Folic Acid

NDC Code 63739-110-01
Proprietary Name Folic Acid
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-110-01) > 30 TABLET in 1 BLISTER PACK
Product NDC 63739-110
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Folic Acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041124
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation.
Substance Name FOLIC ACID
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Folic Acid


General Information