Orange Book product · Generic (ANDA)
METHYLDOPA
METHYLDOPA
At a glance
Oct 09, 1986
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 09, 1986
40 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
METHYLDOPA
Strength
500MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 070074
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of METHYLDOPA
- 1984METHYLDOPABrand (NDA)
NDA 018934 · CHARTWELL RX
- —ALDOMETBrand (NDA)
NDA 018389 · MERCK
- —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
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.
