Escavite

Product NDC

58809-888

11-digit product format

588090888

Labeler code

58809

Product ID

58809-888_935bc301-7376-4676-8ba5-085e4463e5a2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sodium Fluoride, Vitamin A Acetate, Biotin, Magnesium, Zinc, Copper, Calcium Pantothenate, Folic Acid, Iron, ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, and CYANOCOBALAMIN

Dosage form

TABLET, CHEWABLE

Route

ORAL

Labeler

GM Pharmaceuticals, Inc.

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2012-02-01

Marketing end

0000-00-00

Substance

SODIUM FLUORIDE; VITAMIN A ACETATE; BIOTIN; MAGNESIUM; ZINC; COPPER; CALCIUM PANTOTHENATE; FOLIC ACID; IRON; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; CYANOCOBALAMIN

Active strength

0 mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; ug/1

Pharmacologic classes

Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record