Dutasteridedrug info

dutasteride 0.5 MG / tamsulosin hydrochloride 0.4 MG Oral Capsule

What it is used for

Dutasteride and tamsulosin hydrochloride capsules are a combination of dutasteride, a 5-alpha-reductase inhibitor, and tamsulosin, an alpha-adrenergic antagonist, indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate.

Limitations of Use: Dutasteride-containing products, including dutasteride and tamsulosin hydrochloride capsules, are not approved for the prevention of prostate cancer.

1.1 Benign Prostatic

Hyperplasia (BPH) Treatment Dutasteride and tamsulosin hydrochloride capsules are indicated for the treatment of symptomatic BPH in men with an enlarged prostate.

1.2 Limitations of

Use Dutasteride-containing products, including dutasteride and tamsulosin hydrochloride capsules, are not approved for the prevention of prostate cancer.

Text above is quoted in full from the FDA-approved drug label published by openFDA, effective July 19, 2024. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.

Description

Dutasteride and tamsulosin hydrochloride capsules, USP contain dutasteride (a selective inhibitor of both the type 1 and type 2 isoforms of steroid 5 alpha-reductase, an intracellular enzyme that converts testosterone to DHT and tamsulosin (an antagonist of alpha 1A -adrenoceptors in the prostate). Each dutasteride and tamsulosin hydrochloride capsule, USP contains the following: One dutasteride dull-yellow, opaque, oblong shaped soft gelatin capsule containing clear, colorless to pale yellow viscous oil which is 0.5 mg of dutasteride USP dissolved in a mixture of butylated hydroxytoluene and glycerol monocaprylocaprate type I. The inactive ingredients in the soft-gelatin capsule shell are ferric oxide yellow, gelatin (from certified BSE-free bovine sources), glycerin, and titanium dioxide. Tamsulosin hydrochloride white to off-white beadlets, containing 0.4 mg tamsulosin hydrochloride USP and the inactive ingredients: calcium stearate, methacrylic acid and ethyl acrylate copolymer dispersion, microcrystalline cellulose, talc, and triacetin. The above components are encapsulated in a hard-shell capsule made with the inactive ingredients of black iron oxide, carrageenan, FD&C yellow 6, hypromellose, iron oxide red, potassium chloride, and titanium dioxide. The capsules are imprinted with black ink containing black iron oxide, potassium hydroxide, and shellac. Dutasteride: Dutasteride is a synthetic 4-azasteroid compound chemically designated as (5α,17β)-N-{2,5 bis(trifluoromethyl)phenyl}-3-oxo-4-azaandrost-1-ene-17-carboxamide.The molecular formula of dutasteride is C 27 H 30 F 6 N 2 O 2, representing a molecular weight of 528.5 with the following structural formula: Dutasteride is a white to pale yellow powder with a melting point is about 242° to 250ºC. It is soluble in ethanol and in methanol, insoluble in polyethylene glycol 400 and in water. Tamsulosin: Tamsulosin hydrochloride is a synthetic compound chemically designated as (-)-( R )-5-[2-[[2-( o -Ethoxyphenoxy)ethyl]amino]propyl]-2-methoxybenzenesulfonamide, monohydrochloride. The molecular formula of tamsulosin hydrochloride is C 20 H 28 N 2 O 5 S

HCl. The molecular weight of tamsulosin hydrochloride is 444.97. Its structural formula is: Tamsulosin hydrochloride is a white or almost white crystalline powder that melts with decomposition at about 234°C. It is freely soluble in formic acid, sparingly soluble in methanol: slightly soluble in water, very slightly soluble in dehydrated alcohol and practically insoluble in ether. FDA approved dissolution test specifications differ from USP. Chemical Structure 1 Chemical Structure 2

Text above is quoted in full from the FDA-approved drug label published by openFDA, effective July 19, 2024. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.

This page reproduces regulatory text for reference. It is not medical advice, and KenyRx is not a pharmacy or a prescriber. Talk to a doctor or pharmacist about whether a medicine is right for you.

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