Orange Book product · Brand (NDA)
ACTIDIL
TRIPROLIDINE HYDROCHLORIDE
At a glance
Jul 01, 1983
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 01, 1983
43 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
TRIPROLIDINE HYDROCHLORIDE
Strength
1.25MG/5ML
Dosage form
SYRUP
Route
ORAL
TE code
Not listed
Application
NDA 011496
Product number
002
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.
- 1983ACTIDILBrand (NDA)
NDA 011110 · GLAXOSMITHKLINE
- 1985TRIPROLIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 088735 · HALSEY
- 1983MYIDYLGeneric (ANDA)
ANDA 087963 · USL PHARMA
- 1982TRIPROLIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 087514 · PHARM ASSOC
- —TRIPROLIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 085940 · ALPHARMA US PHARMS
- —TRIPROLIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 085610 · VITARINE
- —TRIPROLIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 085094 · 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.
