Orange Book product · Brand (NDA)
ALDOMET
METHYLDOPA
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
METHYLDOPA
Strength
250MG/5ML
Dosage form
SUSPENSION
Route
ORAL
TE code
Not listed
Application
NDA 018389
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.
- 1984METHYLDOPABrand (NDA)
NDA 018934 · CHARTWELL RX
- —ALDOMETBrand (NDA)
NDA 013400 · MERCK
- 1989METHYLDOPAGeneric (ANDA)
ANDA 070669 · SUPERPHARM
- 1989METHYLDOPAGeneric (ANDA)
ANDA 070670 · SUPERPHARM
- 1988METHYLDOPAGeneric (ANDA)
ANDA 072126 · PLIVA
- 1988METHYLDOPAGeneric (ANDA)
ANDA 072127 · PLIVA
- 1988METHYLDOPAGeneric (ANDA)
ANDA 072128 · PLIVA
- 1988METHYLDOPAGeneric (ANDA)
ANDA 071751 · HALSEY
- 1988METHYLDOPAGeneric (ANDA)
ANDA 071752 · HALSEY
- 1988METHYLDOPAGeneric (ANDA)
ANDA 071753 · HALSEY
- 1988METHYLDOPAGeneric (ANDA)
ANDA 071700 · CHARTWELL RX
- 1987METHYLDOPAGeneric (ANDA)
ANDA 070535 · QUAGEN
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.
