Vitafol - 0642-0070-30 - (Prenatal Supplement with DHA)

Alphabetical Index


Drug Information of Vitafol

Product NDC: 0642-0070
Proprietary Name: Vitafol
Non Proprietary Name: Prenatal Supplement with DHA
Active Ingredient(s): 30; 2; .012; 1; .15; 29; 20; 15; 200; 2.5; 1.8; 1.6; 1100; 1000; 20; 25    mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; [iU]/1; mg/1 & nbsp;   Prenatal Supplement with DHA
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Vitafol

Product NDC: 0642-0070
Labeler Name: Everett Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110613

Package Information of Vitafol

Package NDC: 0642-0070-30
Package Description: 5 BLISTER PACK in 1 BOX (0642-0070-30) > 6 CAPSULE, GELATIN COATED in 1 BLISTER PACK

NDC Information of Vitafol

NDC Code 0642-0070-30
Proprietary Name Vitafol
Package Description 5 BLISTER PACK in 1 BOX (0642-0070-30) > 6 CAPSULE, GELATIN COATED in 1 BLISTER PACK
Product NDC 0642-0070
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prenatal Supplement with DHA
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20110613
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Everett Laboratories, Inc.
Substance Name ASCORBIC ACID; COPPER; CYANOCOBALAMIN; FOLIC ACID; IODINE; IRON; MAGNESIUM; NIACIN; OMEGA-3 FATTY ACIDS; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE; VITAMIN A; VITAMIN D; VITAMIN E; ZINC
Strength Number 30; 2; .012; 1; .15; 29; 20; 15; 200; 2.5; 1.8; 1.6; 1100; 1000; 20; 25
Strength Unit mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; [iU]/1; mg/1
Pharmaceutical Classes Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC]

Complete Information of Vitafol


General Information