Source: European Medicines Agency (EU) Revision Year: 2019 Publisher: Teva B.V., Swensweg 5, 2031GA Haarlem, The Netherlands
Nevirapine Teva 200 mg tablets.
| Pharmaceutical Form |
|---|
|
Tablet. White, oval, biconvex tablets. One side is debossed with “N”, a scoreline and “200”. The opposite side is debossed with a scoreline. The score line is only to facilitate breaking for ease of swallowing and not to divide into equal doses. |
Each tablet contains 200 mg of nevirapine (as anhydrous).
Excipient with known effect: Each tablet contains 168 mg of lactose (as monohydrate).
For the full list of excipients, see section 6.1
| Active Ingredient | Description | |
|---|---|---|
| Nevirapine |
Nevirapine is a NNRTI of HIV-1. Nevirapine is a non-competitive inhibitor of the HIV-1 reverse transcriptase, but it does not have a biologically significant inhibitory effect on the HIV-2 reverse transcriptase or on eukaryotic DNA polymerases α, β, γ, or δ. |
| List of Excipients |
|---|
|
Microcrystalline cellulose |
Treatment initiation pack: White opaque PVC/PE/PVdC – Aluminium blisters or OPA/Alu/PVC – Aluminium blisters. Cartons containing 14 tablets (Calendar Pack).
Maintenance packs: White opaque PVC/PE/PVdC – Aluminium blisters or OPA/Alu/PVC – Aluminium blisters. Cartons containing 60 or 120 tablets.
Not all pack sizes may be marketed.
Teva B.V., Swensweg 5, 2031GA Haarlem, The Netherlands
EU/1/09/598/001-006
Date of first authorisation: 30 November 2009
Date of latest renewal: 26 August 2014
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