Orange Book product · Brand (NDA)
NORCURON
VECURONIUM BROMIDE
At a glance
Jan 03, 1992
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 03, 1992
35 yr ago
Today
Pharmaceutical detail
Active ingredient
VECURONIUM BROMIDE
Strength
20MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
NDA 018776
Product number
003
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- 2019VECURONIUM BROMIDEGeneric (ANDA)
ANDA 203725 · HIKMA
- 2018VECURONIUM BROMIDEGeneric (ANDA)
ANDA 206670 · EUGIA PHARMA
- 2016VECURONIUM BROMIDEGeneric (ANDA)
ANDA 205390 · GLAND
- 2010VECURONIUM BROMIDEGeneric (ANDA)
ANDA 090243 · MYLAN LABS LTD
- 2009VECURONIUM BROMIDEGeneric (ANDA)
ANDA 079001 · SUN PHARM
- 2008VECURONIUM BROMIDEGeneric (ANDA)
ANDA 078274 · SAGENT PHARMS INC
- 2001VECURONIUM BROMIDEGeneric (ANDA)
ANDA 075558 · HOSPIRA
- 2000VECURONIUM BROMIDEGeneric (ANDA)
ANDA 075549 · HIKMA
- 1999VECURONIUM BROMIDEGeneric (ANDA)
ANDA 075164 · HOSPIRA
- 1999VECURONIUM BROMIDEGeneric (ANDA)
ANDA 074688 · MEITHEAL
- 1999VECURONIUM BROMIDEGeneric (ANDA)
ANDA 075218 · HIKMA
- 1995VECURONIUM BROMIDEGeneric (ANDA)
ANDA 074334 · 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.
