Orange Book product · Generic (ANDA)
CEFAZOLIN SODIUM
CEFAZOLIN SODIUM
At a glance
Sep 18, 2001
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 18, 2001
25 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
CEFAZOLIN SODIUM
Strength
EQ 1GM BASE/VIAL
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 065047
Product number
002
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of CEFAZOLIN SODIUM
- 2023CEFAZOLIN SODIUMBrand (NDA)
NDA 211413 · HQ SPCLT PHARMA
- 2022CEFAZOLIN SODIUMBrand (NDA)
NDA 216109 · HIKMA
- 2021CEFAZOLIN IN DEXTROSEBrand (NDA)
NDA 207131 · BAXTER HLTHCARE CORP
- 2000CEFAZOLIN AND DEXTROSEBrand (NDA)
NDA 050779 · B BRAUN
- 1983ANCEF IN DEXTROSE 5% IN PLASTIC CONTAINERBrand (NDA)
NDA 050566 · BAXTER HLTHCARE
- —ANCEFBrand (NDA)
NDA 050461 · GLAXOSMITHKLINE
- 2018CEFAZOLIN SODIUMGeneric (ANDA)
ANDA 209217 · QILU ANTIBIOTICS
- 2016CEFAZOLIN SODIUMGeneric (ANDA)
ANDA 201654 · HOSPIRA
- 2015CEFAZOLIN SODIUMGeneric (ANDA)
ANDA 203661 · QILU ANTIBIOTICS
- 2009CEFAZOLIN SODIUMGeneric (ANDA)
ANDA 065280 · CEPHAZONE PHARMA
- 2009CEFAZOLIN SODIUMGeneric (ANDA)
ANDA 065295 · CEPHAZONE PHARMA
- 2009CEFAZOLIN SODIUMGeneric (ANDA)
ANDA 065296 · CEPHAZONE PHARMA
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.
