Orange Book product · Generic (ANDA)
GEMCITABINE HYDROCHLORIDE
GEMCITABINE HYDROCHLORIDE
At a glance
May 07, 2013
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 07, 2013
13 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
GEMCITABINE HYDROCHLORIDE
Strength
EQ 200MG BASE/VIAL
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 202485
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of GEMCITABINE HYDROCHLORIDE
- 2025INLEXZOBrand (NDA)
NDA 219683 · JANSSEN BIOTECH
- 2025AVGEMSIBrand (NDA)
NDA 219920 · AVYXA HOLDINGS
- 2018INFUGEMBrand (NDA)
NDA 208313 · SUN PHARM
- 2017GEMCITABINE HYDROCHLORIDEBrand (NDA)
NDA 209604 · ACCORD HLTHCARE
- 2011GEMCITABINE HYDROCHLORIDEBrand (NDA)
NDA 200795 · HOSPIRA INC
- 1996GEMZARBrand (NDA)
NDA 020509 · LILLY
- 2023GEMCITABINE HYDROCHLORIDEGeneric (ANDA)
ANDA 213175 · HIKMA
- 2021GEMCITABINE HYDROCHLORIDEGeneric (ANDA)
ANDA 206617 · HIKMA INTL PHARMS
- 2020GEMCITABINE HYDROCHLORIDEGeneric (ANDA)
ANDA 212129 · MEITHEAL
- 2019GEMCITABINE HYDROCHLORIDEGeneric (ANDA)
ANDA 210991 · SHILPA
- 2019GEMCITABINE HYDROCHLORIDEGeneric (ANDA)
ANDA 207575 · SHILPA
- 2019GEMCITABINE HYDROCHLORIDEGeneric (ANDA)
ANDA 210383 · INGENUS PHARMS LLC
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.
