Home NDC 69680-183 memantine hydrochloride and donepezil hydrochloride
Product NDC 69680-183
11-digit product format 696800183
Labeler code 69680
Product ID 69680-183_ffe5cf41-299a-49e5-a9b8-c9048c4861fa
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name memantine hydrochloride and donepezil hydrochloride
Dosage form CAPSULE, EXTENDED RELEASE
Route ORAL
Labeler Vitruvias Therapeutics, Inc.
Application ANDA216901
Marketing category ANDA
Marketing start 2025-07-16
Substance DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE
Active strength 10; 14 mg/1; mg/1
Pharmacologic classes Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA], N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]
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 A216901-001 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE 10MG;14MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15 A216901-002 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE 10MG;28MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15
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 2026-02-19 14:30 UTC 2026-02 A216901-001 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE 10MG;14MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A216901-002 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE 10MG;28MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A216901-001 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE 10MG;14MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A216901-002 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE 10MG;28MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A216901-001 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE 10MG;14MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A216901-002 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE 10MG;28MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15 6a471c1ec25d…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A216901-001 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE 10MG;14MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A216901-002 MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE 10MG;28MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-07-15 a50c72e98297…
Observed Orange Book normalized TE history# Additional Listing Data#
Finished product Yes
Brand name base memantine hydrochloride and donepezil hydrochloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MEMANTINE HYDROCHLORIDE 10 mg/1 DONEPEZIL HYDROCHLORIDE 14 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination JY0WD0UA60 Internal UNII lookup 3O2T2PJ89D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1599803 Internal RxNorm lookup 1599805 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 69680-183-30 memantine hydrochloride and donepezil hydrochloride 30 in 1 BOTTLE CAPSULE, EXTENDED RELEASE 30 3
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 69680-183-30 69680018330 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69680-183-30) 2025-07-16 No No Current