NDC 62332-176

Fesoterodine Fumarate

Fesoterodine Fumarate

Fesoterodine Fumarate is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Alembic Pharmaceuticals Inc.. The primary component is Fesoterodine Fumarate.

Product ID62332-176_d347263f-9458-4986-be65-e626f490bb3b
NDC62332-176
Product TypeHuman Prescription Drug
Proprietary NameFesoterodine Fumarate
Generic NameFesoterodine Fumarate
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2023-01-06
Marketing CategoryANDA /
Application NumberANDA204973
Labeler NameAlembic Pharmaceuticals Inc.
Substance NameFESOTERODINE FUMARATE
Active Ingredient Strength8 mg/1
NDC Exclude FlagN
Listing Certified Through2024-12-31

Packaging

NDC 62332-176-10

100 TABLET, EXTENDED RELEASE in 1 CARTON (62332-176-10)
Marketing Start Date2023-01-06
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Fesoterodine Fumarate" or generic name "Fesoterodine Fumarate"

NDCBrand NameGeneric Name
43598-247Fesoterodine fumarateFesoterodine fumarate
43598-248Fesoterodine fumarateFesoterodine fumarate
51407-661Fesoterodine fumarateFesoterodine fumarate
51407-662Fesoterodine fumarateFesoterodine fumarate
62332-175Fesoterodine FumarateFesoterodine Fumarate
62332-176Fesoterodine FumarateFesoterodine Fumarate
62559-376Fesoterodine FumarateFesoterodine Fumarate
65162-369Fesoterodine FumarateFesoterodine Fumarate
65162-370Fesoterodine FumarateFesoterodine Fumarate
65862-766FESOTERODINE FUMARATEFESOTERODINE FUMARATE
68382-479fesoterodine fumaratefesoterodine fumarate
68382-480fesoterodine fumaratefesoterodine fumarate
70771-1168fesoterodine fumaratefesoterodine fumarate
70771-1169fesoterodine fumaratefesoterodine fumarate
0069-0242Toviazfesoterodine fumarate
0069-0244Toviazfesoterodine fumarate
55154-2737Toviazfesoterodine fumarate
55154-2738Toviazfesoterodine fumarate
63539-183Toviazfesoterodine fumarate
63539-242Toviazfesoterodine fumarate
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.