Home NDC 33342-220 Memantine hydrochloride
Product NDC 33342-220
11-digit product format 333420220
Labeler code 33342
Product ID 33342-220_1c695653-b7dd-40af-b5eb-a6e3ecbab14d
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Memantine hydrochloride
Dosage form CAPSULE, EXTENDED RELEASE
Route ORAL
Labeler Macleods Pharmaceuticals Limited
Application ANDA206310
Marketing category ANDA
Marketing start 2025-08-28
Substance MEMANTINE HYDROCHLORIDE
Active strength 14 mg/1
Pharmacologic classes 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 · 4 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A206310-001 MEMANTINE HYDROCHLORIDE MEMANTINE HYDROCHLORIDE 7MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-08-28 A206310-002 MEMANTINE HYDROCHLORIDE MEMANTINE HYDROCHLORIDE 14MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-08-28 A206310-003 MEMANTINE HYDROCHLORIDE MEMANTINE HYDROCHLORIDE 21MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-08-28 A206310-004 MEMANTINE HYDROCHLORIDE MEMANTINE HYDROCHLORIDE 28MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-08-28
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 4 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 A206310-001 MEMANTINE HYDROCHLORIDE 7MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-08-28 a50c72e98297…2026-08-01 22:54:32 2026-06 A206310-002 MEMANTINE HYDROCHLORIDE 14MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-08-28 a50c72e98297…2026-08-01 22:54:32 2026-06 A206310-003 MEMANTINE HYDROCHLORIDE 21MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-08-28 a50c72e98297…2026-08-01 22:54:32 2026-06 A206310-004 MEMANTINE HYDROCHLORIDE 28MG CAPSULE, EXTENDED RELEASE / ORAL AB 2025-08-28 a50c72e98297…
Observed Orange Book normalized TE history# 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 · 1 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base Memantine hydrochloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MEMANTINE HYDROCHLORIDE 14 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination JY0WD0UA60 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 4 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 996594 Internal RxNorm lookup 996603 Internal RxNorm lookup 996609 Internal RxNorm lookup 996615 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 33342-220-07 Memantine hydrochloride 30 in 1 BOTTLE CAPSULE, EXTENDED RELEASE 30 2 33342-220-12 Memantine hydrochloride 10 in 1 BLISTER PACK CAPSULE, EXTENDED RELEASE 10 2 33342-220-12 Memantine hydrochloride 10 in 1 CARTON CAPSULE, EXTENDED RELEASE 10 2
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 33342-220-07 33342022007 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-220-07) 2025-08-28 No No Current 33342-220-12 33342022012 10 BLISTER PACK in 1 CARTON (33342-220-12) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK 10 blister pack 2025-08-28 No No Current