Prenatal Vitamins Plus

Product NDC

70518-1849

11-digit product format

705181849

Labeler code

70518

Product ID

70518-1849_b9427a61-7f18-937f-e053-2995a90a42f9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Vitamin A, Vitamin C, Vitamin D-3, Vitamin E, Vitamin B-1, Vitamin B-2, Niacin, Vitamin B-6, Calcium, Iron, Zinc, Copper

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2019-02-04

Marketing end

0000-00-00

Substance

VITAMIN A ACETATE; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM CARBONATE; FERROUS FUMARATE; ZINC OXIDE; COPPER

Active strength

4000 [iU]/1; mg/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/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],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS],Copper [CS],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE]

NDC exclude flag

No

Listing certified through

2022-12-31

Current FDA listing

Historical FDA.report record