Orange Book product · Generic (ANDA)
ISONIAZID
ISONIAZID
At a glance
Jul 21, 1997
Approved
Generic (ANDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 21, 1997
29 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
ISONIAZID
Strength
50MG/5ML
Dosage form
SYRUP
Route
ORAL
TE code
AA
Application
ANDA 081118
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ISONIAZID
- —NYDRAZIDBrand (NDA)
NDA 008662 · SANDOZ
- —RIMIFONBrand (NDA)
NDA 008420 · ROCHE
- —ISONIAZIDBrand (NDA)
NDA 008678 · EPIC PHARMA LLC
- —ISONIAZIDBrand (NDA)
NDA 008499 · LILLY
- —ISONIAZIDBrand (NDA)
NDA 008428 · PANRAY
- —NYDRAZIDBrand (NDA)
NDA 008392 · BRISTOL MYERS SQUIBB
- 2014ISONIAZIDGeneric (ANDA)
ANDA 202610 · THEPHARMANETWORK LLC
- 2005ISONIAZIDGeneric (ANDA)
ANDA 040648 · SANDOZ
- 1997ISONIAZIDGeneric (ANDA)
ANDA 040090 · OMNIVIUM PHARMS
- 1988LANIAZIDGeneric (ANDA)
ANDA 089776 · CHARTWELL MOLECULAR
- 1986LANIAZIDGeneric (ANDA)
ANDA 089243 · LANNETT
- 1983ISONIAZIDGeneric (ANDA)
ANDA 088235 · CMP PHARMA INC
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.
