Orange Book product · Generic (ANDA)
ENOXAPARIN SODIUM (PRESERVATIVE FREE)
ENOXAPARIN SODIUM
At a glance
Sep 19, 2011
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 19, 2011
15 yr ago
Today
Pharmaceutical detail
Active ingredient
ENOXAPARIN SODIUM
Strength
30MG/0.3ML (100MG/ML)
Dosage form
INJECTABLE
Route
SUBCUTANEOUS
TE code
AP
Application
ANDA 076684
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ENOXAPARIN SODIUM
- 2003LOVENOXBrand (NDA)
NDA 020164 · SANOFI AVENTIS US
- 2026ENOXAPARIN SODIUM (PRESERVATIVE FREE)Generic (ANDA)
ANDA 218775 · HEBEI CHANGSHAN
- 2023ENOXAPARIN SODIUM (PRESERVATIVE FREE)Generic (ANDA)
ANDA 214646 · BE PHARMS
- 2023ENOXAPARIN SODIUM (PRESERVATIVE FREE)Generic (ANDA)
ANDA 205660 · SHENZHEN TECHDOW
- 2022ENOXAPARIN SODIUMGeneric (ANDA)
ANDA 214856 · EMERGE BIOSCIENCE
- 2019ENOXAPARIN SODIUM (PRESERVATIVE FREE)Generic (ANDA)
ANDA 206834 · EMERGE BIOSCIENCE
- 2019ENOXAPARIN SODIUMGeneric (ANDA)
ANDA 208600 · AMPHASTAR PHARMS INC
- 2018ENOXAPARIN SODIUM (PRESERVATIVE FREE)Generic (ANDA)
ANDA 078990 · GLAND
- 2014ENOXAPARIN SODIUM (PRESERVATIVE FREE)Generic (ANDA)
ANDA 076726 · ZYDUS PHARMS
- 2011ENOXAPARIN SODIUMGeneric (ANDA)
ANDA 078660 · SANDOZ INC
- 2010ENOXAPARIN SODIUM (PRESERVATIVE FREE)Generic (ANDA)
ANDA 077857 · SANDOZ
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.
