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

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CYPROHEPTADINE HYDROCHLORIDE

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

CYPROHEPTADINE HYDROCHLORIDE DESCRIPTION



CYPROHEPTADINE HYDROCHLORIDE



CLINICAL PHARMACOLOGY


PHARMACOKINETICS AND METABOLISM


INDICATIONS & USAGE









PRECAUTIONS

General






CYPROHEPTADINE HYDROCHLORIDE CONTRAINDICATIONS

Newborn or Premature Infants


Nursing Mothers


Other Conditions








WARNINGS

Pediatric Patients



CNS Depressants


Activities Requiring Mental Alertness

PRECAUTIONS, Geriatric Use).

INFORMATION FOR PATIENTS


DRUG INTERACTIONS



CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY




PREGNANCY



NURSING MOTHERS

CONTRAINDICATIONS).

PEDIATRIC USE

CONTRAINDICATIONS, Newborn or Premature Infants,andWARNINGS, Pediatric Patients).

GERIATRIC USE

WARNINGS, Activities Requiring Mental Alertness).

CYPROHEPTADINE HYDROCHLORIDE ADVERSE REACTIONS



Central Nervous System


Integumentary


Special Senses


Cardiovascular


Hematologic


Digestive System


Genitourinary


Respiratory


Miscellaneous

OVERDOSAGE









DOSAGE & ADMINISTRATION




Pediatric Patients

Age 2 to 6 years



Age 7 to 14 years


Adults

HOW SUPPLIED


STORAGE AND HANDLING




PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














CYPROHEPTADINE HYDROCHLORIDE




CYPROHEPTADINE HYDROCHLORIDE

CYPROHEPTADINE HYDROCHLORIDE

CYPROHEPTADINE HYDROCHLORIDE TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:52125-014(NDC:0093-2929)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CYPROHEPTADINE CYPROHEPTADINE 4 mg

Inactive Ingredients

Ingredient Name Strength
cellulose, microcrystalline
lactose monohydrate
MAGNESIUM STEARATE
SODIUM STARCH GLYCOLATE TYPE A POTATO

Product Characteristics

Color Size Imprint Code Shape
white 7 mm 2929;93 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52125-014-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA087056 2012-08-16


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Be sure to consult your doctor before taking any medication!
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