Orange Book product · Generic (ANDA)
NIACIN
NIACIN
At a glance
Approved Prior to Jan 1, 1982
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
NIACIN
Strength
500MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 083453
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of NIACIN
- 1997NIASPANBrand (NDA)
NDA 020381 · ABBVIE
- —WAMPOCAPBrand (NDA)
NDA 011073 · MEDPOINTE PHARM HLC
- 2025NIACINGeneric (ANDA)
ANDA 207726 · MPP PHARMA
- 2025NIACINGeneric (ANDA)
ANDA 203285 · ZYDUS PHARMS
- 2023NIACINGeneric (ANDA)
ANDA 213090 · HIBROW HLTHCARE
- 2022NIACINGeneric (ANDA)
ANDA 204934 · MACLEODS PHARMS LTD
- 2021NIACINGeneric (ANDA)
ANDA 214428 · BEIJING
- 2019NIACINGeneric (ANDA)
ANDA 212017 · YICHANG HUMANWELL
- 2019NIACINGeneric (ANDA)
ANDA 203742 · RISING
- 2018NIACINGeneric (ANDA)
ANDA 209156 · JUBILANT GENERICS
- 2018NIACINGeneric (ANDA)
ANDA 209236 · AUROBINDO PHARMA LTD
- 2017NIACINGeneric (ANDA)
ANDA 203899 · LANNETT CO INC
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.
