Marketing-authorisation holder · United States
Teva Branded Pharm
38 medicines in 1 country, as authorisation holder.
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Marketing-authorisation holder · United States
38 medicines in 1 country, as authorisation holder.
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Groups are put together by Prognia from the names regulators publish and from company links; they are not an official corporate structure.
Every medicine in the registers under its name, current ones first.
1–25 of 38
| Medicine | Substance | Country | Status | Authorised |
|---|---|---|---|---|
| ACTIGALL150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 300MG · Capsule | Ursodeoxycholic acid | United States | Marketed | 1987 |
| AUSTEDO12mg | 6mg | 9mg · Tablet | Deutetrabenazine | United States | Marketed | 2017 |
| CONDYLOX0.5% · Solution | Podofilox | United States | Not marketed | 1990 |
| DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet | Acetazolamide | United States | Not marketed | 1953 |
| DIAMOX500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Capsule, extended release | Acetazolamide | United States | Not marketed | 1962 |
| EMLA2.5%; 2.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Cream | Lidocaine, Prilocaine | United States | Not marketed | 1992 |
| LOESTRIN 21 1/200.02MG; 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet | Ethinyl estradiol, Norethindrone | United States | Not marketed | 1976 |
| LOESTRIN 21 1.5/300.03mg; 1.5mg · Tablet | Ethinyl estradiol, Norethindrone | United States | Not marketed | 1976 |
| LOESTRIN 24 FE0.02MG; 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet | Ethinyl estradiol, Norethindrone | United States | Not marketed | 2006 |
| LOESTRIN FE 1/200.02MG; 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet | Ethinyl estradiol, Norethindrone | United States | Not marketed | 1973 |
| LOESTRIN FE 1.5/300.03mg; 1.5mg · Tablet | Ethinyl estradiol, Norethindrone | United States | Not marketed | 1973 |
| LOSEASONIQUE0.02mg,0.1mg; 0.01mg,n/a · Tablet | Ethinyl estradiol, Levonorgestrel, N/a | United States | Marketed | 2008 |
| LOXITANE10MG BASE **Federal Register determination that product was discontinued or withdrawn for s or e reasons** | 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet | Loxapine | United States | Not marketed | 1975 |
| LOXITANE10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 5MG BASE * · Capsule | Loxapine | United States | Not marketed | 1975 |
| LOXITANE C25mg base/ml · Concentrate | Loxapine | United States | Not marketed | 1976 |
| MICROZIDE12.5mg · Capsule | Hydrochlorothiazide | United States | Marketed | 1996 |
| MIRCETTE0.15MG,N/A; 0.02MG,0.01MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet | Desogestrel, N/a, Ethinyl estradiol | United States | Not marketed | 1998 |
| NASAREL0.029mg/spray · Spray, metered | Flunisolide | United States | Not marketed | 1995 |
| NOR-QD0.35mg · Tablet | Norethindrone | United States | Marketed | 1973 |
| NORDETTE-210.03mg; 0.15mg · Tablet | Ethinyl estradiol, Levonorgestrel | United States | Not marketed | 1982 |
| NORDETTE-280.03MG; 0.15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet | Ethinyl estradiol, Levonorgestrel | United States | Not marketed | 1982 |
| PREVEN EMERGENCY CONTRACEPTIVE KIT0.05mg; 0.25mg · Tablet | Ethinyl estradiol, Levonorgestrel | United States | Not marketed | 1998 |
| PROAIR DIGIHALER0.09mg base/inh · Powder, metered | Salbutamol | United States | Not marketed | 2015 |
| PROAIR HFA0.09mg base/inh · Aerosol, metered | Salbutamol | United States | Marketed | 2004 |
| PROAIR RESPICLICK0.09mg base/inh · Powder, metered | Salbutamol | United States | Marketed | 2015 |
Where it holds or makes medicines, with how many are current.
| Country | Medicines | Current | Past | Companies |
|---|---|---|---|---|
| United States | 38 | 38 | 0 | CompaniesAll medicines |
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)
Report an error or request removalCorrections from the company itself are welcome.
Other companies in the same group.
Ranked by their number of medicines.