Orange Book product · Generic (ANDA)
NAFCILLIN SODIUM
NAFCILLIN SODIUM
At a glance
Dec 23, 1986
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 23, 1986
40 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
NAFCILLIN SODIUM
Strength
EQ 1GM BASE/VIAL
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 062732
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of NAFCILLIN SODIUM
- 1989NALLPEN IN PLASTIC CONTAINERBrand (NDA)
NDA 050655 · BAXTER HLTHCARE
- —UNIPENBrand (NDA)
NDA 050111 · WYETH AYERST
- —UNIPENBrand (NDA)
NDA 050199 · WYETH AYERST
- —UNIPENBrand (NDA)
NDA 050320 · WYETH AYERST
- —UNIPENBrand (NDA)
NDA 050462 · WYETH AYERST
- 2020NAFCILLIN SODIUMGeneric (ANDA)
ANDA 206761 · FRESENIUS
- 2019NAFCILLIN SODIUMGeneric (ANDA)
ANDA 206682 · FRESENIUS
- 2014NAFCILLIN SODIUMGeneric (ANDA)
ANDA 200002 · ONESOURCE SPECIALTY
- 2012NAFCILLIN SODIUMGeneric (ANDA)
ANDA 091613 · EUGIA PHARMA SPECLTS
- 2012NAFCILLIN SODIUMGeneric (ANDA)
ANDA 091614 · EUGIA PHARMA SPECLTS
- 2012NAFCILLIN SODIUMGeneric (ANDA)
ANDA 090582 · SAGENT PHARMS
- 2012NAFCILLIN SODIUMGeneric (ANDA)
ANDA 090580 · SAGENT PHARMS
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.

