TRICARE PRENATAL DHA ONE RX

Product NDC

67112-402

Requested package NDC

67112-402-30

11-digit product format

671120402

Labeler code

67112

Product ID

67112-402_4952d7c5-0c2e-4cf0-8bcf-a1cab52b9bfe

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

FISH OIL, DHA, EPA, VITAMINS B-1, B-2, B-3, B-6, B-12, C, D3, E, BIOTIN, IRON, ZINC, COPPER, IODINE, DOCUSATE SODIUM

Dosage form

CAPSULE, GELATIN COATED

Route

ORAL

Labeler

Medecor Pharma, LLC

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2019-03-15

Marketing end

0000-00-00

Substance

FISH OIL; DOCONEXENT; ICOSAPENT; THIAMINE MONONITRATE; RIBOFLAVIN; INOSITOL NIACINATE; PYRIDOXINE HYDROCHLORIDE; CYANOCOBALAMIN; FOLIC ACID; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL, D-; BIOTIN; FERROUS FUMARATE; ZINC SULFATE MONOHYDRATE; CUPRIC SULFATE ANHYDROUS; POTASSIUM IODIDE; DOCUSATE SODIUM

Active strength

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

Pharmacologic classes

Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE],Vitamin B 12 [CS],Vitamin B12 [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record