Orange Book product · Brand (NDA)
HYDERGINE LC
ERGOLOID MESYLATES
At a glance
Jan 18, 1983
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 18, 1983
44 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
ERGOLOID MESYLATES
Strength
1MG
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
NDA 018706
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.
- —HYDERGINEBrand (NDA)
NDA 018418 · NOVARTIS
- —HYDERGINEBrand (NDA)
NDA 017993 · NOVARTIS
- —HYDERGINEBrand (NDA)
NDA 009087 · NOVARTIS
- 1991ERGOLOID MESYLATESGeneric (ANDA)
ANDA 081113 · SUN PHARM INDUSTRIES
- 1986ERGOLOID MESYLATESGeneric (ANDA)
ANDA 089233 · SUPERPHARM
- 1986ERGOLOID MESYLATESGeneric (ANDA)
ANDA 089234 · SUPERPHARM
- 1985ERGOLOID MESYLATESGeneric (ANDA)
ANDA 088891 · MUTUAL PHARM
- 1984GERIMALGeneric (ANDA)
ANDA 088207 · WATSON LABS
- 1982ERGOLOID MESYLATESGeneric (ANDA)
ANDA 088013 · VANGARD
- 1982ERGOLOID MESYLATESGeneric (ANDA)
ANDA 088014 · VANGARD
- 1982ERGOLOID MESYLATESGeneric (ANDA)
ANDA 087244 · WATSON LABS
- 1982ERGOLOID MESYLATESGeneric (ANDA)
ANDA 086433 · WATSON LABS
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.
