Home NDC 62332-176 Fesoterodine Fumarate
Product NDC 62332-176
11-digit product format 623320176
Labeler code 62332
Product ID 62332-176_2fc9ba3f-2336-45b8-9020-bffc1298a6e0
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Fesoterodine Fumarate
Dosage form TABLET, EXTENDED RELEASE
Route ORAL
Labeler Alembic Pharmaceuticals Inc.
Application ANDA204973
Marketing category ANDA
Marketing start 2023-01-06
Substance FESOTERODINE FUMARATE
Active strength 8 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A204973-001 FESOTERODINE FUMARATE FESOTERODINE FUMARATE 4MG TABLET, EXTENDED RELEASE / ORAL AB 2023-01-04 A204973-002 FESOTERODINE FUMARATE FESOTERODINE FUMARATE 8MG TABLET, EXTENDED RELEASE / ORAL AB 2023-01-04
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 matching rows.
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-01 22:54:32 2026-06 A204973-001 FESOTERODINE FUMARATE 4MG TABLET, EXTENDED RELEASE / ORAL AB 2023-01-04 a50c72e98297…2026-08-01 22:54:32 2026-06 A204973-002 FESOTERODINE FUMARATE 8MG TABLET, EXTENDED RELEASE / ORAL AB 2023-01-04 a50c72e98297…
Observed Orange Book normalized TE history# Captured, Edition, Application-product table Captured Edition Application-product TE code Order Source SHA-256 2026-08-01 22:54:32 2026-06 A204973-001 AB 1 a50c72e98297…2026-08-01 22:54:32 2026-06 A204973-002 AB 1 a50c72e98297…
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 2 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base Fesoterodine Fumarate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FESOTERODINE FUMARATE 8 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination EOS72165S7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 810071 Internal RxNorm lookup 810077 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62332-176-10 Fesoterodine Fumarate 100 in 1 CARTON TABLET, EXTENDED RELEASE 100 8 62332-176-30 Fesoterodine Fumarate 30 in 1 BOTTLE TABLET, EXTENDED RELEASE 30 8 62332-176-90 Fesoterodine Fumarate 90 in 1 BOTTLE TABLET, EXTENDED RELEASE 90 8 62332-176-91 Fesoterodine Fumarate 1000 in 1 BOTTLE TABLET, EXTENDED RELEASE 1000 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62332-176 FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE [ALEMBIC PHARMACEUTICALS INC.] 7 Current NDC, Legacy NDC, 4 package rows 20240810_299db62d-9658-4796-b449-657fa859c5cd.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 62332-176-10 62332017610 100 TABLET, EXTENDED RELEASE in 1 CARTON (62332-176-10) 2023-01-06 0000-00-00 No No Current 62332-176-30 62332017630 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-176-30) 2023-01-06 0000-00-00 No No Current 62332-176-90 62332017690 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-176-90) 2023-01-06 0000-00-00 No No Current 62332-176-91 62332017691 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-176-91) 2023-01-06 0000-00-00 No No Current