Orange Book product · Generic (ANDA)
TRIPROLIDINE HYDROCHLORIDE
TRIPROLIDINE HYDROCHLORIDE
At a glance
Jan 17, 1985
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 17, 1985
42 yr ago
Today
Pharmaceutical detail
Active ingredient
TRIPROLIDINE HYDROCHLORIDE
Strength
1.25MG/5ML
Dosage form
SYRUP
Route
ORAL
TE code
Not listed
Application
ANDA 088735
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of TRIPROLIDINE HYDROCHLORIDE
- 1983ACTIDILBrand (NDA)
NDA 011496 · GLAXOSMITHKLINE
- 1983ACTIDILBrand (NDA)
NDA 011110 · GLAXOSMITHKLINE
- 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.
