Orange Book product · Generic (ANDA)
FOLIC ACID
FOLIC ACID
At a glance
Feb 18, 1986
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 18, 1986
40 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
FOLIC ACID
Strength
5MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 089202
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
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
- 2014FOLIC ACIDGeneric (ANDA)
ANDA 202437 · CADILA PHARMS LTD
- 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
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.
