Orange Book product · Generic (ANDA)
METHOTREXATE SODIUM
METHOTREXATE SODIUM
At a glance
Oct 11, 1985
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 11, 1985
41 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
METHOTREXATE SODIUM
Strength
EQ 50MG BASE/VIAL
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 088936
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of METHOTREXATE SODIUM
- 2017XATMEPBrand (NDA)
NDA 208400 · AZURITY
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ANDA 219865 · HETERO LABS LTD VI
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ANDA 220225 · ALEMBIC
- 2024METHOTREXATE SODIUMGeneric (ANDA)
ANDA 217552 · ALEMBIC
- 2024METHOTREXATE SODIUMGeneric (ANDA)
ANDA 216453 · ELITE LABS INC
- 2023METHOTREXATE SODIUMGeneric (ANDA)
ANDA 213362 · DAITO
- 2021METHOTREXATE SODIUMGeneric (ANDA)
ANDA 209787 · LOTUS PHARM CO LTD
- 2020METHOTREXATE SODIUMGeneric (ANDA)
ANDA 210454 · EUGIA PHARMA
- 2020METHOTREXATE SODIUMGeneric (ANDA)
ANDA 213343 · ACCORD HLTHCARE
- 2018METHOTREXATE SODIUM PRESERVATIVE FREEGeneric (ANDA)
ANDA 203407 · SAGENT PHARMS INC
- 2017METHOTREXATE SODIUMGeneric (ANDA)
ANDA 210040 · AMNEAL 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.
