Orange Book product · Generic (ANDA)
ORPHENADRINE CITRATE
ORPHENADRINE CITRATE
At a glance
Apr 06, 1983
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 06, 1983
43 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
ORPHENADRINE CITRATE
Strength
100MG
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
TE code
Not listed
Application
ANDA 088067
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ORPHENADRINE CITRATE
- —NORFLEXBrand (NDA)
NDA 013055 · PAI HOLDINGS PHARM
- —NORFLEXBrand (NDA)
NDA 012157 · BAUSCH
- 2012ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 091158 · UNICHEM
- 2011ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 090585 · SAGENT PHARMS
- 2006ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 040484 · RISING
- 2003ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 040463 · HIKMA
- 2000ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 040368 · STEVENS J
- 2000ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 040327 · SANDOZ
- 1999ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 040249 · RISING
- 1998ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 040284 · LUPIN
- 1982ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 084779 · WATSON LABS
- —ORPHENADRINE CITRATEGeneric (ANDA)
ANDA 087062 · 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.
