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Bimatoprost 10mg  | Purity Not Available

Selleck Chemicals

Bimatoprost(AGN 192024) is a prostaglandin analog used topically (as eye drops) to control the progression of glaucoma and in the management of ocular hypertension.

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Bimatoprost 50mg  | Purity Not Available

Selleck Chemicals

Bimatoprost(AGN 192024) is a prostaglandin analog used topically (as eye drops) to control the progression of glaucoma and in the management of ocular hypertension.

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Alfuzosin HCl 10mg  | Purity Not Available

Selleck Chemicals

Alfuzosin HCI(SL 77499 HCl) is an alpha1 receptor antagonist used to treat benign prostatic hyperplasia (BPH).

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Stavudine (d4T) 25mg  | Purity Not Available

Selleck Chemicals

Stavudine (d4T, BMY-27857, Sanilvudine, NSC 163661) is a nucleoside analog reverse transcriptase inhibitor (NARTI) active against HIV.

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Stavudine (d4T) 100mg  | Purity Not Available

Selleck Chemicals

Stavudine (d4T, BMY-27857, Sanilvudine, NSC 163661) is a nucleoside analog reverse transcriptase inhibitor (NARTI) active against HIV.

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Teicoplanin 50mg  | Purity Not Available

Selleck Chemicals

Teicoplanin (Teichomycin,Targocid,MDL-507) is a glycopeptide antibiotic, used to treat serious infections caused by Gram-positive bacteria.

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Tenofovir Disoproxil Fumarate 10mg  | Purity Not Available

Selleck Chemicals

Tenofovir Disoproxil Fumarate belongs to a class of antiretroviral drugs, it inhibits the activity of HIV reverse transcriptase by competing with the natural substrate deoxyadenosine 5’-triphosphate and, after incorporation into DNA, by DNA chain termination.

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Tenofovir Disoproxil Fumarate 50mg  | Purity Not Available

Selleck Chemicals

Tenofovir Disoproxil Fumarate belongs to a class of antiretroviral drugs, it inhibits the activity of HIV reverse transcriptase by competing with the natural substrate deoxyadenosine 5’-triphosphate and, after incorporation into DNA, by DNA chain termination.

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Tenofovir Disoproxil Fumarate 10mM/1mL  | Purity Not Available

Selleck Chemicals

Tenofovir Disoproxil Fumarate belongs to a class of antiretroviral drugs, it inhibits the activity of HIV reverse transcriptase by competing with the natural substrate deoxyadenosine 5’-triphosphate and, after incorporation into DNA, by DNA chain termination.

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