Marketing-authorisation holder
Hetero Drugs Ltd
3 medicines in 1 country, as authorisation holder and manufacturer.
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Marketing-authorisation holder
3 medicines in 1 country, as authorisation holder and manufacturer.
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Every medicine in the registers under its name, current ones first.
3 medicines
| Medicine | Substance | Country | Status | Authorised |
|---|---|---|---|---|
| LAMIVUDINE, NEVIRAPINE, AND STAVUDINE150mg; 200mg; 30mg Β· Tablet | Lamivudine, Nevirapine, Stavudine | United States | tentative | 2010 |
| LAMIVUDINE/TENOFOVIR DISOPROXIL FUMARATE FDC TABS300mg/300mg Β· Tablet | Lamivudine, Tenofovir disoproxil | United States | tentative | 2009 |
| LAMIVUDINE, ZIDOVUDINE TABS 150MG/300MG CO-PACKAGED WITH NEVIRAPINE TABS 200MG150mg; 300mg; 200mg Β· Tablet | Lamivudine, Zidovudine, Nevirapine | United States | tentative | 2009 |
Where it holds or makes medicines, with how many are current.
| Country | Medicines | Current | Past | Companies |
|---|---|---|---|---|
| United States | 3 | 0 | 3 | CompaniesAll medicines |
Also in the registers of Brazil
The active substances in most of its medicines.
How the registers spell it, normalised: legal forms, accents and capitals removed.
Compiled by Prognia from the public medicine and company registers below. Logos are not used.
Source: U.S. FDA, Drugs@FDA / openFDA. FDA does not endorse this site.
Licence: Public domain (U.S. Government work)
Anvisa, official medicine/API manufacturer factual export, HTTP source version Fri, 09 Oct 2026 08:21:54 GMT, acquired 2026-10-09; exact unmodified native identifiers and fields preserved.
Licence: Brazil federal factual open-data reuse; Decreto 8777/2016 consolidated article 4 and third-party exceptions
Report an error or request removalCorrections from the company itself are welcome.