DIVALPROEX SODIUM | A078790 | LUPIN LTD
No patent or exclusivity listings for this strength.
Lupin's divalproex sodium (Depakote) product (NDA 078790) transitioned from prescription (RX) to discontinued (DISCN) status.
Old: RX
New: DISCN
Lupin's divalproex sodium (NDA 078790, supplement 002) therapeutic equivalence code changed from AB to a different rating.
Old: AB
Lupin's divalproex sodium (NDA 078790) therapeutic equivalence code changed from AB to another rating.
Old: AB
Lupin's Divalproex Sodium (divalproex sodium) product revised its therapeutic equivalence rating from AB to a different code.
Old: AB
Lupin's divalproex sodium product (NDA 078790, supplement 002) status changed from prescription to discontinued.
Old: RX
New: DISCN
Lupin's divalproex sodium (Depakote) tablet formulation was discontinued, changing its status from prescription to discontinued in the FDA Orange Book.
Old: RX
New: DISCN