Orange Book product · Generic (ANDA)
TOBRAMYCIN
TOBRAMYCIN
At a glance
Jun 28, 2017
Approved
Generic (ANDA)
Application
AT
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 28, 2017
9 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
TOBRAMYCIN
Strength
0.3%
Dosage form
SOLUTION/DROPS
Route
OPHTHALMIC
TE code
AT
Application
ANDA 207444
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of TOBRAMYCIN
- 2014KITABIS PAKBrand (NDA)
NDA 205433 · PULMOFLOW INC
- 2013TOBI PODHALERBrand (NDA)
NDA 201688 · VIATRIS
- 2012BETHKISBrand (NDA)
NDA 201820 · CHIESI
- 1997TOBIBrand (NDA)
NDA 050753 · VIATRIS
- —TOBREXBrand (NDA)
NDA 050555 · NOVARTIS
- —TOBREXBrand (NDA)
NDA 050541 · NOVARTIS
- 2023TOBRAMYCINGeneric (ANDA)
ANDA 217344 · MICRO LABS
- 2023TOBRAMYCINGeneric (ANDA)
ANDA 214478 · MANKIND PHARMA
- 2022TOBRAMYCINGeneric (ANDA)
ANDA 216725 · MANKIND PHARMA
- 2021TOBRAMYCINGeneric (ANDA)
ANDA 212848 · ALKEM LABS LTD
- 2021TOBRAMYCINGeneric (ANDA)
ANDA 212628 · GLAND
- 2021TOBRAMYCINGeneric (ANDA)
ANDA 210871 · LUOXIN AUROVITAS
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.
