NDC 67877-068

Fesoterodine Fumarate

Fesoterodine Fumarate

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

Product ID67877-068_ded7636a-4d3b-4738-8772-4b823c30896d
NDC67877-068
Product TypeHuman Prescription Drug
Proprietary NameFesoterodine Fumarate
Generic NameFesoterodine Fumarate
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2022-06-09
Marketing CategoryANDA /
Application NumberANDA204827
Labeler NameAscend Laboratories, LLC
Substance NameFESOTERODINE FUMARATE
Active Ingredient Strength8 mg/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 67877-068-30

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-068-30)
Marketing Start Date2022-06-09
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
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.