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Nevirapine (CAS No.: 129618-40-2)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Nevirapine, 129618-40-2.
We offer the product Nevirapine, 129618-40-2 from our manufacturer / supplier / principals for your Research and Development / Evaluation or Commercial requirements, based on the product's availability from our network. We can also offer Nevirapine, 129618-40-2 intermediates with the supportive technical package required for evaluation.
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CAS number:

129618-40-2

Chemical Name:

Viramune; 11-Cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one , Nevirapine (CAS No.: 129618-40-2)

Pharmacopeia:

USP, EP, CP, In House

Manufacturer Certificate:

GMP - SFDA, cGMP, EUGMP, WHO GMP, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

Viramune; 11-Cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one , Nevirapine (CAS No.: 129618-40-2)

Molecular Formula

C15H14N4O

Molecular Weight

266.30

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Product Name	CAS No.
2-Chloro-N-(2-chloro-4-methylpyridin-3-yl)nicotinamide	133627-46-0	View \| Inquire
2-Chloro-3-amino-4-methyl pyridine	133627-45-9	View \| Inquire

Description:

Nevirapine (NVP), marketed under the trade name Viramune, is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used to treat HIV-1 infection and AIDS.

Manufacturer Documentation / Approvals :

USDMF	EDMF	CEP / COS

Products protected by valid patents from a manufacturer are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use from a manufacturer in accordance with 35 USC 271 +A13(1)
Products falling in to controlled substance category / list of schedule drugs shall be exported directly from the manufacturer principals only against receipt of original import permission issued by concerned authorities of the importing country.
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