Orange Book product · Brand (NDA)
VIDEX
DIDANOSINE
At a glance
Oct 09, 1991
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 09, 1991
35 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
DIDANOSINE
Strength
100MG/PACKET
Dosage form
FOR SOLUTION
Route
ORAL
TE code
Not listed
Application
NDA 020155
Product number
003
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 2000VIDEX ECBrand (NDA)
NDA 021183 · BRISTOL MYERS SQUIBB
- 1991VIDEXBrand (NDA)
NDA 020156 · BRISTOL
- 1991VIDEXBrand (NDA)
NDA 020154 · BRISTOL MYERS SQUIBB
- 2012DIDANOSINEGeneric (ANDA)
ANDA 077275 · AUROBINDO
- 2010DIDANOSINEGeneric (ANDA)
ANDA 090788 · PHARMOBEDIENT
- 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.
