Orange Book product · Generic (ANDA)
DIDANOSINE
DIDANOSINE
At a glance
Apr 08, 2010
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 08, 2010
16 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
DIDANOSINE
Strength
125MG
Dosage form
CAPSULE, DELAYED REL PELLETS
Route
ORAL
TE code
Not listed
Application
ANDA 090788
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of DIDANOSINE
- 2000VIDEX ECBrand (NDA)
NDA 021183 · BRISTOL MYERS SQUIBB
- 1991VIDEXBrand (NDA)
NDA 020156 · BRISTOL
- 1991VIDEXBrand (NDA)
NDA 020155 · BRISTOL MYERS SQUIBB
- 1991VIDEXBrand (NDA)
NDA 020154 · BRISTOL MYERS SQUIBB
- 2012DIDANOSINEGeneric (ANDA)
ANDA 077275 · AUROBINDO
- 2008DIDANOSINEGeneric (ANDA)
ANDA 090094 · AUROBINDO PHARMA
- 2007DIDANOSINEGeneric (ANDA)
ANDA 078112 · AUROBINDO PHARMA
- 2004DIDANOSINEGeneric (ANDA)
ANDA 077167 · BARR
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.
