Vitafol

Product NDC
0642-0072
11-digit product format
006420072
Labeler code
0642
Product ID
0642-0072_667440e5-a115-41f7-91a7-8acf0edc115f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Vitamin A, Ascorbic Acid, Vitamin D, .Alpha.-Tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium, and Iron
Dosage form
CAPSULE
Route
ORAL
Labeler
Everett Laboratories, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
1985-05-01
Marketing end
0000-00-00
Substance
VITAMIN A; ASCORBIC ACID; VITAMIN D; .ALPHA.-TOCOPHEROL; THIAMINE MONONITRATE; RIBOFLAVIN; NIACIN; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM; IRON
Active strength
6000 [iU]/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1
Pharmacologic classes
Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Nicotinic Acid [EPC],Nicotinic Acids [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Calcium [CS],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0642-0072-122023-01-09C16284748780-19d75b9d0-741d-f424-e053-dadaa90a57ced4713072-1864-40ce-b003-a171fb2bc127
0642-0072-122020-01-31C16284748780-19d75b9d0-741d-f424-e053-dadaa90a57ced4713072-1864-40ce-b003-a171fb2bc127

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0642-0072-12EA - Each0642-00725bf141f6-3d40-4cfc-8e48-b8b9708bcb6912014-10-03