Orange Book product · Generic (ANDA)
CYPROHEPTADINE HYDROCHLORIDE
CYPROHEPTADINE HYDROCHLORIDE
At a glance
Nov 29, 2016
Approved
Generic (ANDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 29, 2016
9 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
CYPROHEPTADINE HYDROCHLORIDE
Strength
4MG
Dosage form
TABLET
Route
ORAL
TE code
AA
Application
ANDA 206553
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
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.
