Orange Book product · Generic (ANDA)
PROMETHAZINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE
DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE
At a glance
Jul 31, 1996
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 31, 1996
30 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE
Strength
15MG/5ML;6.25MG/5ML
Dosage form
SYRUP
Route
ORAL
TE code
Not listed
Application
ANDA 040027
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE
- 1984PROMETHAZINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDEBrand (NDA)
NDA 011265 · ANI PHARMS
- 2026PROMETHAZINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDEGeneric (ANDA)
ANDA 218264 · HETERO LABS LTD III
- 2012PROMETHAZINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDEGeneric (ANDA)
ANDA 091687 · COSETTE PHARMS NC
- 2011PROMETHAZINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDEGeneric (ANDA)
ANDA 090575 · AMNEAL PHARMS
- 2006PROMETHAZINE DMGeneric (ANDA)
ANDA 040649 · PAI HOLDINGS
- 1987PHERAZINE DMGeneric (ANDA)
ANDA 088913 · HALSEY
- 1985PROMETHAZINE W/ DEXTROMETHORPHANGeneric (ANDA)
ANDA 088864 · PHARMOBEDIENT
- 1984PROMETH W/ DEXTROMETHORPHANGeneric (ANDA)
ANDA 088762 · G AND W LABS INC
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.
