Orange Book product · Generic (ANDA)
CYPROHEPTADINE HYDROCHLORIDE
CYPROHEPTADINE HYDROCHLORIDE
At a glance
Jun 28, 2006
Approved
Generic (ANDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 28, 2006
20 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
CYPROHEPTADINE HYDROCHLORIDE
Strength
2MG/5ML
Dosage form
SYRUP
Route
ORAL
TE code
AA
Application
ANDA 040668
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of CYPROHEPTADINE HYDROCHLORIDE
- —PERIACTINBrand (NDA)
NDA 013220 · MERCK
- —PERIACTINBrand (NDA)
NDA 012649 · MERCK
- 2021CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 205431 · TRIS PHARMA INC
- 2021CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 212491 · QUAGEN
- 2019CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 212423 · QUAGEN
- 2019CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 206676 · REGCON HOLDINGS
- 2018CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 209108 · ST JOHN PHARM
- 2018CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 209172 · STRIDES PHARMA INTL
- 2017CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 203191 · CHARTWELL MOLECULAR
- 2017CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 208938 · ZYDUS PHARMS
- 2017CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 207555 · RISING
- 2016CYPROHEPTADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 207783 · RISING
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.
