Orange Book product · Generic (ANDA)
ACARBOSE
ACARBOSE
At a glance
Feb 07, 2012
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 07, 2012
14 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
ACARBOSE
Strength
25MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 202271
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ACARBOSE
- 1997PRECOSEBrand (NDA)
NDA 020482 · BAYER HLTHCARE
- 2020ACARBOSEGeneric (ANDA)
ANDA 213821 · HANGZHOU ZHONGMEI
- 2013ACARBOSEGeneric (ANDA)
ANDA 091343 · SOMERSET THERAPS LLC
- 2011ACARBOSEGeneric (ANDA)
ANDA 090912 · STRIDES PHARMA
- 2011ACARBOSEGeneric (ANDA)
ANDA 091053 · NATCO PHARMA USA
- 2009ACARBOSEGeneric (ANDA)
ANDA 078441 · IMPAX LABS
- 2008ACARBOSEGeneric (ANDA)
ANDA 078470 · HIKMA
- 2008ACARBOSEGeneric (ANDA)
ANDA 077532 · 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.
