TriphroCaps description, usages, side effects, indications, overdosage, supplying and lots more!

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TriphroCaps

State of Florida DOH Central Pharmacy

TriphroCaps Softgels


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Rx Only

TRIPHROCAPS DESCRIPTION

TriphroCaps are an orally administered prescription vitamin for the dietary management of patients with nutritional deficiencies or are in need of nutritional supplementation. TriphroCaps are red, oval softgel capsules, imprinted "T9."

Supplement Facts
Servings per Bottle: 100
Serving Size: 1 Softgel Capsule
Each Softgel Capsule contains
%DV Adults & Children
4 Years or More
Folate 1 mg 250%
Vitamin C (ascorbic acid) 100 mg 167%
Niacin (niacinamide) 20 mg 100%
Thiamine (thiamine mononitrate) 1.5 mg 100%
Riboflavin 1.7 mg 100%
Vitamin B6 (pyridoxine HCl) 10 mg 500%
Vitamin B12 (cyanocobalamin) 6 mcg 100%
Pantothenic Acid (calcium pantothenate) 5 mg 50%
Biotin 150 mcg 50%

Inactive Ingredients: Soybean Oil, Gelatin, Glycerin, Purified Water, Yellow Bees Wax, Lecithin, Titanium Dioxide, FD&C Red #40, Ethyl Vanillin, FD&C Yellow #5, FD&C Yellow #6, Iron Oxide.

TRIPHROCAPS INDICATIONS AND USAGE

TriphroCaps are indicated for the supplemental requirements of patients with nutritional deficiencies or are in need of nutritional supplementation.

TriphroCaps are an orally administered prescription vitamin for the dietary management of patients with nutritional deficiencies or are in need of nutritional supplementation.

TRIPHROCAPS CONTRAINDICATIONS

TriphroCaps is contraindicated in patients with a known hypersensitivity to any of the ingredients.

WARNINGS

Folic acid alone is improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where Vitamin B12 is deficient. Folic acid in doses above 0.1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations remain progressive.

THIS PRODUCT CONTAINS SOY.

PRECAUTIONS

Pediatric Use

Safety and effectiveness in pediatric patients have not been established.

Geriatric Use

Clinical studies on this product have not been performed in sufficient numbers of subjects aged 65 and over to determine whether elderly subjects respond differently from younger subjects. In general, dose selection for elderly patients should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function of concomitant disease or other drug therapy.

TRIPHROCAPS ADVERSE REACTIONS

Allergic sensitization has been reported following both oral and parenteral administration of folic acid.

TRIPHROCAPS DOSAGE AND ADMINISTRATION

Take one TriphroCaps softgel daily or as prescribed by a physician. On dialysis days, take one TriphroCaps softgel after dialysis.

HOW SUPPLIED

TriphroCaps are supplied in bottles of 100 softgel capsules.

They are supplied by State of Florida DOH Central Pharmacy as follows:

NDC Quantity/Form Color Source Prod. Code
53808-0987-1 30 Capsules in a Blister Pack RED 13811-525

STORAGE

Store at 20°-25°C (68°-77°F), excursions permitted to 15°-30°C (59°-86°F) [See USP controlled room temperature].

Call your doctor about side effects. You may report side effects by calling 888 9 TRIGEN (888-987-4436).

KEEP OUT OF REACH OF CHILDREN

Rx Only

All prescriptions using this product shall be pursuant to state statutes as applicable. This is not an Orange Book product. There are no implied or explicit claims on therapeutic equivalence.

Manufactured for:
TRIGEN Laboratories, Inc., Sayreville, NJ 08872
www.trigenlab.com

This Product was Repackaged By:

State of Florida DOH Central Pharmacy
104-2 Hamilton Park Drive
Tallahassee, FL 32304
United States

PACKAGE LABEL

Label Image for 53808-0987

TriphroCaps

TriphroCaps

folic acid, ascorbic acid, niacinamide, thiamine mononitrate, riboflavin, pyridoxine Hydrochloride, cyanocobalamin, calcium pantothenate, and biotin CAPSULE

Product Information

Product Type Dietary supplement Item Code (Source) NDC:53808-0987(NDC:13811-525)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FOLIC ACID FOLIC ACID 1 mg
ASCORBIC ACID ASCORBIC ACID 100 mg
NIACINAMIDE 20 mg
THIAMINE MONONITRATE THIAMINE ION 1.5 mg
RIBOFLAVIN RIBOFLAVIN 1.7 mg
PYRIDOXINE HYDROCHLORIDE PYRIDOXINE 10 mg
Cyanocobalamin CYANOCOBALAMIN 6 ug
CALCIUM PANTOTHENATE PANTOTHENIC ACID 5 mg
BIOTIN 150 ug

Inactive Ingredients

Ingredient Name Strength
SOYBEAN OIL
GELATIN
GLYCERIN
water
YELLOW WAX
titanium dioxide
FD&C RED NO. 40
ETHYL VANILLIN
FD&C YELLOW NO. 5
FD&C YELLOW NO. 6
ferric oxide red

Product Characteristics

Color Size Imprint Code Shape
RED 13 mm T9 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:53808-0987-1 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-01-01


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