Folic Acid - 0615-0664-31 - (Folic Acid)

Alphabetical Index


Drug Information of Folic Acid

Product NDC: 0615-0664
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: 0615-0664
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080600
Marketing Category: ANDA
Start Marketing Date: 19720331

Package Information of Folic Acid

Package NDC: 0615-0664-31
Package Description: 31 TABLET in 1 BLISTER PACK (0615-0664-31)

NDC Information of Folic Acid

NDC Code 0615-0664-31
Proprietary Name Folic Acid
Package Description 31 TABLET in 1 BLISTER PACK (0615-0664-31)
Product NDC 0615-0664
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Folic Acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19720331
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name FOLIC ACID
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Folic Acid


General Information