Orange Book product · Generic (ANDA)
NAPROXEN SODIUM
NAPROXEN SODIUM
At a glance
Dec 21, 1993
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 21, 1993
33 yr ago
Today
Pharmaceutical detail
Active ingredient
NAPROXEN SODIUM
Strength
EQ 250MG BASE
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 074162
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of NAPROXEN SODIUM
- 2006NAPROXEN SODIUMBrand (NDA)
NDA 021920 · BIONPHARMA
- 1996NAPRELANBrand (NDA)
NDA 020353 · TWI PHARMS
- 1994ALEVEBrand (NDA)
NDA 020204 · BAYER
- —ANAPROXBrand (NDA)
NDA 018164 · ATNAHS PHARMA US
- 2023NAPROXEN SODIUMGeneric (ANDA)
ANDA 214463 · PATHEON SOFTGELS
- 2022NAPROXEN SODIUMGeneric (ANDA)
ANDA 211065 · HETERO LABS LTD V
- 2022NAPROXEN SODIUMGeneric (ANDA)
ANDA 215472 · ONESOURCE SPECIALTY
- 2019NAPROXEN SODIUMGeneric (ANDA)
ANDA 212199 · SCIEGEN PHARMS
- 2019NAPROXEN SODIUMGeneric (ANDA)
ANDA 212033 · YICHANG HUMANWELL
- 2019NAPROXEN SODIUMGeneric (ANDA)
ANDA 202807 · CATALENT
- 2018NAPROXEN SODIUMGeneric (ANDA)
ANDA 207612 · NOVELGENIX THERAPS
- 2018NAPROXEN SODIUMGeneric (ANDA)
ANDA 208363 · PURACAP PHARM 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.

