Orange Book product · Brand (NDA)
MEFLOQUINE HYDROCHLORIDE
MEFLOQUINE HYDROCHLORIDE
At a glance
May 02, 1989
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 02, 1989
37 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
MEFLOQUINE HYDROCHLORIDE
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
NDA 019578
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 1989LARIAMBrand (NDA)
NDA 019591 · ROCHE
- 2010MEFLOQUINE HYDROCHLORIDEGeneric (ANDA)
ANDA 077699 · HIKMA INTL PHARMS
- 2004MEFLOQUINE HYDROCHLORIDEGeneric (ANDA)
ANDA 076523 · HIKMA
- 2003MEFLOQUINE HYDROCHLORIDEGeneric (ANDA)
ANDA 076392 · BARR
- 2002MEFLOQUINE HYDROCHLORIDEGeneric (ANDA)
ANDA 076175 · CHARTWELL RX
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
