drugmine

phenytoin-sodium


Name: PHENYTOIN SODIUM
ID :
MW: 251
Number of atoms: 19
Molecular_Formula: C15H11N2O2
Alogp: 2.084
Indication class : Anticonvulsant
Oral Flag : 1
Max_Phase : 4
Molecule_Type : Small molecule

phenytoin sodium containing products summary

There are in total 35 different products containing the active ingredient phenytoin sodium. From the 35 drug products, 19 have been discontinued.

Product id = 7236
Application Number = 10151
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = DILANTIN
Route/format = INJECTION / INJECTABLE
Application Type = N
Applicant Name = PARKE DAVIS
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----
Product id = 1902
Application Number = 40298
Date of Application = 28,, Dec, 1998
RX/OTC/DISCN = RX
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = MYLAN
ProductNo = 001
Tecode = AB
Rld = No
Strength = 100MG EXTENDED
----
Product id = 2890
Application Number = 40298
Date of Application = 6,, Dec, 2001
RX/OTC/DISCN = RX
Tradename = PHENYTEK
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = MYLAN
ProductNo = 002
Tecode = AB
Rld = No
Strength = 200MG EXTENDED
----
Product id = 2891
Application Number = 40298
Date of Application = 6,, Dec, 2001
RX/OTC/DISCN = RX
Tradename = PHENYTEK
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = MYLAN
ProductNo = 003
Tecode = AB
Rld = Yes
Strength = 300MG EXTENDED
----
Product id = 1900
Application Number = 40435
Date of Application = 20,, Jun, 2003
RX/OTC/DISCN = DISCN
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = ANI PHARMS INC
ProductNo = 001
Tecode =
Rld = No
Strength = 100MG EXTENDED
----
Product id = 10123
Application Number = 40573
Date of Application = 13,, Sep, 2006
RX/OTC/DISCN = RX
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = X-GEN PHARMS
ProductNo = 001
Tecode = AP
Rld = No
Strength = 50MG/ML
----
Product id = 1905
Application Number = 40621
Date of Application = 11,, Dec, 2006
RX/OTC/DISCN = RX
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = SUN PHARM INDS (IN)
ProductNo = 001
Tecode = AB
Rld = No
Strength = 100MG EXTENDED
----
Product id = 1906
Application Number = 40684
Date of Application = 5,, Sep, 2006
RX/OTC/DISCN = RX
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = TARO
ProductNo = 001
Tecode = AB
Rld = No
Strength = 100MG EXTENDED
----
Product id = 1903
Application Number = 40731
Date of Application = 30,, Jun, 2008
RX/OTC/DISCN = RX
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = SUN PHARM INDS
ProductNo = 001
Tecode = AB
Rld = No
Strength = 200MG EXTENDED
----
Product id = 1904
Application Number = 40731
Date of Application = 30,, Jun, 2008
RX/OTC/DISCN = RX
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = SUN PHARM INDS
ProductNo = 002
Tecode = AB
Rld = No
Strength = 300MG EXTENDED
----
Product id = 1908
Application Number = 40732
Date of Application = 30,, Jan, 2008
RX/OTC/DISCN = RX
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = WOCKHARDT USA
ProductNo = 001
Tecode = AB
Rld = No
Strength = 100MG EXTENDED
----
Product id = 1907
Application Number = 40759
Date of Application = 18,, Dec, 2007
RX/OTC/DISCN = RX
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = WOCKHARDT
ProductNo = 001
Tecode = AB
Rld = No
Strength = 30MG EXTENDED
----
Product id = 1899
Application Number = 40765
Date of Application = 12,, Nov, 2008
RX/OTC/DISCN = RX
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = AMNEAL PHARMS NY
ProductNo = 001
Tecode = AB
Rld = No
Strength = 100MG EXTENDED
----
Product id = 10115
Application Number = 40781
Date of Application = 4,, Dec, 2007
RX/OTC/DISCN = RX
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = LUITPOLD
ProductNo = 001
Tecode = AP
Rld = No
Strength = 50MG/ML
----
Product id = 3042
Application Number = 80259
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = PROMPT PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = ANI PHARMS INC
ProductNo = 001
Tecode =
Rld = No
Strength = 100MG PROMPT
----
Product id = 1669
Application Number = 80857
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = DIPHENYLAN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = LANNETT
ProductNo = 001
Tecode =
Rld = No
Strength = 30MG PROMPT
----
Product id = 1670
Application Number = 80857
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = DIPHENYLAN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = LANNETT
ProductNo = 002
Tecode =
Rld = No
Strength = 100MG PROMPT
----
Product id = 3043
Application Number = 80905
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = PROMPT PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = WATSON LABS
ProductNo = 001
Tecode =
Rld = No
Strength = 100MG PROMPT
----
Product id = 10111
Application Number = 84307
Date of Application = Prior, Approved, to
RX/OTC/DISCN = RX
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = EUROHLTH INTL SARL
ProductNo = 001
Tecode = AP
Rld = Yes
Strength = 50MG/ML
----
Product id = 1606
Application Number = 84349
Date of Application = Prior, Approved, to
RX/OTC/DISCN = RX
Tradename = DILANTIN
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = PARKE DAVIS
ProductNo = 001
Tecode = AB
Rld = Yes
Strength = 30MG EXTENDED
----
Product id = 1607
Application Number = 84349
Date of Application = Prior, Approved, to
RX/OTC/DISCN = RX
Tradename = DILANTIN
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = PARKE DAVIS
ProductNo = 002
Tecode = AB
Rld = Yes
Strength = 100MG EXTENDED
----
Product id = 10122
Application Number = 85434
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = WATSON LABS
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----
Product id = 2893
Application Number = 85435
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = PHARMERAL
ProductNo = 001
Tecode =
Rld = No
Strength = 100MG PROMPT
----
Product id = 2894
Application Number = 85894
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = WATSON LABS
ProductNo = 001
Tecode =
Rld = No
Strength = 100MG PROMPT
----
Product id = 10118
Application Number = 88519
Date of Application = 19,, Dec, 1984
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = SMITH AND NEPHEW
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----
Product id = 10120
Application Number = 88520
Date of Application = 17,, Dec, 1984
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = SOLOPAK
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----
Product id = 10119
Application Number = 88521
Date of Application = 18,, Dec, 1984
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = SMITH AND NEPHEW
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----
Product id = 2892
Application Number = 88711
Date of Application = 21,, Dec, 1984
RX/OTC/DISCN = DISCN
Tradename = PHENYTEX
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = WATSON LABS
ProductNo = 001
Tecode =
Rld = No
Strength = 100MG EXTENDED
----
Product id = 10112
Application Number = 89003
Date of Application = 31,, May, 1985
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = FRESENIUS KABI USA
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----
Product id = 1901
Application Number = 89441
Date of Application = 18,, Dec, 1986
RX/OTC/DISCN = DISCN
Tradename = EXTENDED PHENYTOIN SODIUM
Route/format = ORAL / CAPSULE
Application Type = A
Applicant Name = ANI PHARMS INC
ProductNo = 001
Tecode =
Rld = No
Strength = 100MG EXTENDED
----
Product id = 10116
Application Number = 89501
Date of Application = 13,, Oct, 1987
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = MARSAM PHARMS LLC
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----
Product id = 10113
Application Number = 89521
Date of Application = 17,, Mar, 1987
RX/OTC/DISCN = RX
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = HOSPIRA
ProductNo = 001
Tecode = AP
Rld = No
Strength = 50MG/ML
----
Product id = 10114
Application Number = 89744
Date of Application = 18,, Dec, 1987
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = HOSPIRA
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----
Product id = 10117
Application Number = 89779
Date of Application = 27,, Nov, 1992
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = MARSAM PHARMS LLC
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----
Product id = 10121
Application Number = 89900
Date of Application = 30,, Mar, 1990
RX/OTC/DISCN = DISCN
Tradename = PHENYTOIN SODIUM
Route/format = INJECTION / INJECTABLE
Application Type = A
Applicant Name = WARNER CHILCOTT
ProductNo = 001
Tecode =
Rld = No
Strength = 50MG/ML
----