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

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Ferrous Sulfate

Boca Pharmacal, LLC
Boca Pharmacal, LLC




FULL PRESCRIBING INFORMATION

Supplement Facts

Serving Size: 1 Tablet
Amount Per Tablet % Daily Value
Iron 65 mg 361 %

Other ingredients: Calcium phosphate, cellulose, croscarmellose sodium, FD&C red #40, hypromellose, magnesium stearate, mineral oil, polyethylene glycol, sodium starch glycolate, stearic acid (veg. grade), talc, and titanium dioxide.

Formula: Each tablet contains 200 mg of dried ferrous sulfate USP (65 mg of elemental iron), equivalent to 325 mg of ferrous sulfate USP.

Directions: Adults and children over 12 years of age: 1 tablet daily as a dietary supplement, preferably with a meal or as directed by a doctor. Do not exceed 2 tablets in 24 hours. Not for frequent or prolonged use except on the advice of a doctor. Do not give to children under 12 years of age. Do not exceed recommended dosage.

Caution: Since oral iron products interfere with absorption of certain antibiotics, these products should not be taken within two hours of each other. If you are pregnant, nursing or taking any medications, consult your doctor before use. Discontinue use and consult your doctor if any adverse reactions occur.

STORE AT 20°- 25°C (68° - 77°F); Excursions permitted to 15°- 30°C (59° - 86°F), see USP Controlled Room Temperature. Store away from heat and moisture. Keep tightly closed.

Tamper resistant: Do not use if seal under cap is broken or missing.

Manufactured for:
Boca Pharmacal, LLC
Coral Springs, FL 33065
www.bocapharmacal.com
1-800-354-8460
Rev. 09/13

Warning: Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. Keep this product out of the reach of children. In case of accidental overdose, call a doctor or poison control center immediately.

Ferrous Sulfate Tablets, USP 325mg

1000ct

NDC: 64376-809-10

Ferrous Sulfate

[Rev. 10]

Ferrous Sulfate

Iron TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:64376-809
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FERROUS SULFATE FERROUS CATION 65 mg

Inactive Ingredients

Ingredient Name Strength
talc
titanium dioxide
HYPROMELLOSES
MAGNESIUM STEARATE
POLYETHYLENE GLYCOLS
Mineral Oil
CALCIUM PHOSPHATE
CROSCARMELLOSE SODIUM
FD&C RED NO. 40
POWDERED CELLULOSE
STEARIC ACID
SODIUM STARCH GLYCOLATE TYPE A POTATO

Product Characteristics

Color Size Shape
RED 10 mm ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64376-809-10 1000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2010-09-14


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