Home NDC 0642-0094 Vitafol
Product NDC 0642-0094
11-digit product format 006420094
Labeler code 0642
Product ID 0642-0094_0777c9df-4100-45c4-a591-4343901b5347
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name CHOLECALCIFEROL, Pyridoxine Hydrochloride, Folic Acid, Levomefolate Calcium, Cyanocobalamin, Iron, and Iodine
Dosage form TABLET, COATED
Route ORAL
Labeler Exeltis USA, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2014-07-14
Marketing end 0000-00-00
Substance CHOLECALCIFEROL; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; LEVOMEFOLATE CALCIUM; CYANOCOBALAMIN; IRON; IODINE
Active strength 25 ug/1; mg/1; ug/1; ug/1; ug/1; mg/1; ug/1
Pharmacologic classes Vitamin D [CS],Vitamin D [EPC],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC]
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0642-0094-01 00642009401 30 TABLET, COATED in 1 BOTTLE (0642-0094-01) 2014-07-14 0000-00-00 No No Current 0642-0094-03 00642009403 3 TABLET, COATED in 1 BLISTER PACK (0642-0094-03) 2014-07-14 0000-00-00 No No Current