Orange Book product · Generic (ANDA)
DIMENHYDRINATE
DIMENHYDRINATE
At a glance
Approved Prior to Jan 1, 1982
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
DIMENHYDRINATE
Strength
50MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 080841
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of DIMENHYDRINATE
- 2004DIMENHYDRINATEGeneric (ANDA)
ANDA 040519 · FRESENIUS KABI USA
- —DIMENHYDRINATEGeneric (ANDA)
ANDA 084767 · BAXTER HLTHCARE
- —DIMENHYDRINATEGeneric (ANDA)
ANDA 083531 · WATSON LABS
- —DIMENHYDRINATEGeneric (ANDA)
ANDA 080615 · WATSON LABS TEVA
- —DIMENHYDRINATEGeneric (ANDA)
ANDA 084316 · WYETH AYERST
- —DIMENHYDRINATEGeneric (ANDA)
ANDA 080715 · ALRA
- —DIMENHYDRINATEGeneric (ANDA)
ANDA 085985 · NEXGEN PHARMA INC
- —DIMENHYDRINATEGeneric (ANDA)
ANDA 085166 · 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.
