Orange Book product · Brand (NDA)
ACTIFED
PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
At a glance
Jun 17, 1985
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 17, 1985
41 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
Strength
120MG;5MG
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
TE code
Not listed
Application
NDA 018996
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.
- 1991TRIPROLIDINE AND PSEUDOEPHEDRINE HYDROCHLORIDESGeneric (ANDA)
ANDA 072758 · KV PHARM
- 1989TRIPROLIDINE AND PSEUDOEPHEDRINE HYDROCHLORIDESGeneric (ANDA)
ANDA 071798 · KV PHARM
- 1985CORPHEDGeneric (ANDA)
ANDA 088602 · CHARTWELL RX
- 1985TRIPROLIDINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDEGeneric (ANDA)
ANDA 088578 · SUPERPHARM
- 1985TRILITRONGeneric (ANDA)
ANDA 088474 · NEWTRON PHARMS
- 1985ALLERFEDGeneric (ANDA)
ANDA 088860 · PVT FORM
- 1985TRILITRONGeneric (ANDA)
ANDA 088515 · NEWTRON PHARMS
- 1984TRIPROLIDINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDEGeneric (ANDA)
ANDA 085273 · IVAX SUB TEVA PHARMS
- 1984TRIPHEDGeneric (ANDA)
ANDA 088630 · TEVA
- 1984HISTAFEDGeneric (ANDA)
ANDA 088283 · CENCI
- 1984ACTAHISTGeneric (ANDA)
ANDA 088344 · CENCI
- 1984TRIPROLIDINE AND PSEUDOEPHEDRINEGeneric (ANDA)
ANDA 088318 · 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.
