FOLIC ACID - 76282-210-10 - (FOLIC ACID)

Alphabetical Index


Drug Information of FOLIC ACID

Product NDC: 76282-210
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: 76282-210
Labeler Name: Exelan Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090035
Marketing Category: ANDA
Start Marketing Date: 20100406

Package Information of FOLIC ACID

Package NDC: 76282-210-10
Package Description: 1000 TABLET in 1 BOTTLE (76282-210-10)

NDC Information of FOLIC ACID

NDC Code 76282-210-10
Proprietary Name FOLIC ACID
Package Description 1000 TABLET in 1 BOTTLE (76282-210-10)
Product NDC 76282-210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FOLIC ACID
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100406
Marketing Category Name ANDA
Labeler Name Exelan Pharmaceuticals, Inc.
Substance Name FOLIC ACID
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of FOLIC ACID


General Information