Orange Book product · Generic (ANDA)
CHLORDIAZEPOXIDE HYDROCHLORIDE
CHLORDIAZEPOXIDE HYDROCHLORIDE
At a glance
Approved Prior to Jan 1, 1982
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Strength
5MG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 084678
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of CHLORDIAZEPOXIDE HYDROCHLORIDE
- 1988CHLORDIAZEPOXIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 089533 · PIONEER PHARMS
- 1988CHLORDIAZEPOXIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 089558 · PIONEER PHARMS
- 1985CHLORDIAZEPOXIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 088987 · SUPERPHARM
- 1985CHLORDIAZEPOXIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 088986 · SUPERPHARM
- 1982CHLORDIAZEPOXIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 087525 · ASCOT
- 1982CHLORDIAZEPOXIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 087524 · ASCOT
- 1982CHLORDIAZEPOXIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 087512 · ASCOT
- —A-POXIDEGeneric (ANDA)
ANDA 085447 · ABBOTT
- —A-POXIDEGeneric (ANDA)
ANDA 085517 · ABBOTT
- —A-POXIDEGeneric (ANDA)
ANDA 085518 · ABBOTT
- —A-POXIDEGeneric (ANDA)
ANDA 085513 · ABBOTT
- —CHLORDIAZACHELGeneric (ANDA)
ANDA 085086 · RACHELLE
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.
