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FERROUS SULFATE

Unit Dose Services
Unit Dose Services

FERROUS SULFATE TABLETS 325 mg (5 gr)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Serving Size: 1 Tablet
Amount per Tablet
% Daily Value
Iron (as ferrous sulfate)  65 mg 360 %

One (1) tablet daily, preferably after meals or as directed by the doctor. As directed by the doctor. Adults: Children:

U.S. RDA* EACH TABLET CONTAINS:                  %

Elemental Iron 65 mg     360

(Equivalent to 325 mg of Ferrous Sulfate)

* U.S. Recommended Daily Allowance  

Croscarmellose sodium, dicalcium phosphate, FD&C RED#40 (Al-lake), FD&C yellow #6 (Al-lake), hypromellose, magnesium stearate, microcrystalline cellulose, PEG 400, titanium dioxide

Iron Supplement

Accidental overdose of iron containing products is a leading cause of fatal poisoning in children under 6. . In case of accidental overdose, call a doctor or Poison Control Center immediately. Keep this product out of reach of children

The treatment of any anemic condition should be under the advice and supervision of doctor. Occasional gastrointestinal discomfort (such as nausea) may be minimized by taking with meals. Iron-containing medication may occasionally cause constipation or diarrhea. WARNINGS: Do not exceed recommended dosage.

As with any drug, if you are pregnant or nursing baby, seek the advice of a health professional before using this product.   

Since oral iron products interfere with absorption of oral tetracycline antibiotics , these products should not be taken within two hours of each other.

Calcium 20 mg (2% daily value) Store in a dry place at controlled room temperature at 15-30 °C (59°-86° F). Do not expose to excessive heat or moisture. Each tablet contains:

DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP OR BAND AROUND ANY CAPSULE IS MISSING OR DAMAGED

TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS BROKEN OR DAMAGED

Distributed by: Qualitest Pharmaceuticals, Inc.

FERROUS SULFATE (IRON SUPPLEMENT) TABLET

FERROUS SULFATE

FERROUS SULFATE

IRON SUPPLEMENT TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50436-5890(NDC:0603-0179)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FERROUS SULFATE FERROUS CATION 325 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE
FD&C RED NO. 40
FD&C YELLOW NO. 6
HYPROMELLOSES
MAGNESIUM STEARATE
cellulose, microcrystalline
polyethylene glycol 400
titanium dioxide

Product Characteristics

Color Size Shape
RED 8 mm ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50436-5890-1 30 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2001-02-19


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Be sure to consult your doctor before taking any medication!
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