Orange Book product · Generic (ANDA)
NALIDIXIC ACID
NALIDIXIC ACID
At a glance
Jun 29, 1988
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 29, 1988
38 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
NALIDIXIC ACID
Strength
500MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 070271
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of NALIDIXIC ACID
- —NEGGRAMBrand (NDA)
NDA 017430 · SANOFI AVENTIS US
- —NEGGRAMBrand (NDA)
NDA 014214 · SANOFI AVENTIS US
- 1988NALIDIXIC ACIDGeneric (ANDA)
ANDA 070272 · SUN PHARM INDUSTRIES
- 1988NALIDIXIC ACIDGeneric (ANDA)
ANDA 070270 · SUN PHARM INDUSTRIES
- 1988NALIDIXIC ACIDGeneric (ANDA)
ANDA 071919 · WATSON LABS
- 1988NALIDIXIC ACIDGeneric (ANDA)
ANDA 071936 · WATSON LABS
- 1988NALIDIXIC ACIDGeneric (ANDA)
ANDA 072061 · 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.
