Friday, February 13, 2009

RE-Nata 29 OB Prenatal Vitamin Tablets





Dosage Form: tablet
RE-Nata 29 OB Prenatal Vitamin Tablets

DESCRIPTION:


RE-Nata 29 OB Prenatal Vitamin Tablets are prescription prenatal vitamins.




INACTIVE INGREDIENTS:


RE-Nata 29 OB Prenatal Vitamins Tablets also contain carnauba wax, croscarmellose sodium, dicalcium phosphate, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, stearic acid, titanium dioxide.

INDICATIONS AND USAGE:


RE-Nata 29 OB Prenatal Vitamin Tablets are indicated to provide vitamin and mineral supplementation throughout pregnancy and during postnatal period for the lactating and non-lactating mother. It is also useful for improving the nutritional status prior to conception.


RE-Nata 29 OB Prenatal Vitamin Tablets contain 1 mg folic acid, which is very important in the development of the baby’s spinal column, especially during the first trimester. Women are advised to start taking folate supplementation several weeks before conception and to continue taking them through the first 12 weeks of pregnancy, or longer. It is recommended that all women of childbearing years take supplements containing folic acid.

CONTRAINDICATIONS:


RE-Nata 29 OB Prenatal Vitamin Tablets are contraindicated in patients with known hypersensitivity to any of its ingredients. Folic acid (pteroylglutamic acid) is contraindicated in patients with untreated and uncomplicated pernicious anemia, and in those with anaphylactic sensitivity to folic acid. Iron therapy is contraindicated in patients with hemochromatosis and patients with iron storage disease or the potential for iron storage disease due to chronic hemolytic anemia (e.g., inherited anomalies of hemoglobin structure or synthesis and/or red cell enzyme deficiencies, etc.), pyridoxine responsive anemia or cirrhosis of the liver.



WARNINGS:


Pernicious anemia should be ruled out before starting treatment. While folic acid corrects the hematological profile of pernicious anemia, it does not ameliorate the underlying neurologic involvement.



PRECAUTIONS:


General: Before prescribing to patients with kidney stones, the calcium content should be considered. Folic acid may partially correct the hematological damage due to deficiency of pernicious anemia, while the associated neurological damage progresses. In rare instances allergic sensitization has been reported following both oral and parenteral administration of folic acid.


Pediatric Use: Safety and effectiveness in children has not been established.



ADVERSE REACTIONS:


Allergic sensitivity reactions and gastrointestinal disturbances may occur. By taking RE-Nata 29 OB Prenatal Vitamin Tablets shortly after meals, G.I. disturbances may be controlled.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.



DOSAGE AND ADMINISTRATION:


One tablet daily, or as directed by physician.



HOW SUPPLIED:


RE-Nata 29 OB Prenatal Vitamin Tablets are supplied as round, white tablets, debossed with “RE 394,” in bottles of 90 tablets (NDC # 68032-394-90). Dispense in a tight, light-resistant container with a child resistant closure as defined by the USP.



STORAGE:


Store at controlled room temperature 15°–30°C (59°–86°F). Protect from moisture and excessive heat.


KEEP THIS AND ALL MEDICATIONS OUT OF REACH OF CHILDREN.


Mfd. for:

River’s Edge Pharmaceuticals, LLC

Suwanee, GA 30024

Rev. 04/09 394-11



PACKAGING:










RE NATA OB  
beta carotene, ascorbic acid, cholecalciferol, alpha-tocopherol, thiamine mononitrate, riboflavin, niacinamide, pyridoxine hydrochloride, folic acid, cyanocobalamin, biotin, pantothenic acid, calcium carbonate, iron pentacarbonyl, potassium iodide, zinc oxide, cupric oxide, magnesium oxide  tablet










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)68032-394
Route of AdministrationORALDEA Schedule    



























































Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BETA CAROTENE (BETA CAROTENE)BETA CAROTENE4000 [iU]
ASCORBIC ACID (ASCORBIC ACID)ASCORBIC ACID120 mg
CHOLECALCIFEROL (CHOLECALCIFEROL)CHOLECALCIFEROL400 [iU]
ALPHA-TOCOPHEROL (ALPHA-TOCOPHEROL)ALPHA-TOCOPHEROL30 [iU]
THIAMINE MONONITRATE (THIAMINE)THIAMINE MONONITRATE3 mg
RIBOFLAVIN (RIBOFLAVIN)RIBOFLAVIN3 mg
NIACINAMIDE (NIACINAMIDE)NIACINAMIDE20 mg
PYRIDOXINE HYDROCHLORIDE (PYRIDOXINE)PYRIDOXINE HYDROCHLORIDE3 mg
FOLIC ACID (FOLIC ACID)FOLIC ACID1 mg
CYANOCOBALAMIN (CYANOCOBALAMIN)CYANOCOBALAMIN8 ug
BIOTIN (BIOTIN)BIOTIN30 ug
PANTOTHENIC ACID (PANTOTHENIC ACID)PANTOTHENIC ACID7 mg
CALCIUM CARBONATE (CALCIUM)CALCIUM CARBONATE200 mg
IRON PENTACARBONYL (IRON)IRON PENTACARBONYL29 mg
POTASSIUM IODIDE (POTASSIUM CATION)POTASSIUM IODIDE150 ug
ZINC OXIDE (ZINC)ZINC OXIDE15 mg
CUPRIC OXIDE (CUPRIC OXIDE)CUPRIC OXIDE3 mg
MAGNESIUM OXIDE (MAGNESIUM)MAGNESIUM OXIDE100 mg






















Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
CROSCARMELLOSE SODIUM 
ANHYDROUS DIBASIC CALCIUM PHOSPHATE 
HYPROMELLOSES 
MAGNESIUM STEARATE 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOL 
STEARIC ACID 
TITANIUM DIOXIDE 


















Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize8mm
FlavorImprint CodeRE;394
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
168032-394-9090 TABLET In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/14/200906/30/2012


Labeler - River's Edge Pharmaceuticals, LLC (133879135)
Revised: 04/2011River's Edge Pharmaceuticals, LLC




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