Orange Book product · Generic (ANDA)
FOLIC ACID
FOLIC ACID
At a glance
Jan 27, 2014
Approved
Generic (ANDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 27, 2014
12 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
FOLIC ACID
Strength
1MG
Dosage form
TABLET
Route
ORAL
TE code
AA
Application
ANDA 202437
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of FOLIC ACID
- 2026QUIOFICBrand (NDA)
NDA 216395 · SOLUBIOMIX
- —FOLVITEBrand (NDA)
NDA 005897 · WYETH PHARMS INC
- —FOLIC ACIDBrand (NDA)
NDA 006135 · LILLY
- 2019FOLIC ACIDGeneric (ANDA)
ANDA 202522 · XGEN PHARMS
- 2019FOLIC ACIDGeneric (ANDA)
ANDA 211064 · RISING
- 2015FOLIC ACIDGeneric (ANDA)
ANDA 204418 · NUVO PHARMS INC
- 2013FOLIC ACIDGeneric (ANDA)
ANDA 091145 · AIPING PHARM INC
- 2010FOLIC ACIDGeneric (ANDA)
ANDA 040756 · PH HEALTH
- 2009FOLIC ACIDGeneric (ANDA)
ANDA 090035 · CHARTWELL MOLECULAR
- 2009FOLIC ACIDGeneric (ANDA)
ANDA 040796 · LEADING
- 2005FOLIC ACIDGeneric (ANDA)
ANDA 040625 · AMNEAL PHARM
- 2005FOLIC ACIDGeneric (ANDA)
ANDA 040582 · SUN PHARM INDUSTRIES
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.
