Home NDC 21695-232 Namenda
Product NDC 21695-232
11-digit product format 216950232
Labeler code 21695
Product ID 21695-232_74ce605d-b493-4b95-9d59-9253f81f4e20
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name memantine hydrochloride
Dosage form TABLET
Route ORAL
Labeler Rebel Distributors Corp
Application NDA021487
Marketing category NDA
Marketing start 2006-08-09
Marketing end 0000-00-00
Substance MEMANTINE HYDROCHLORIDE
Active strength 5 mg/1
Pharmacologic classes NMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC]
NDC exclude flag E
Listing certified through 2017-12-31
Current FDA listing Historical FDA.report record 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 N021487-001 NAMENDA MEMANTINE HYDROCHLORIDE 5MG TABLET / ORAL RLD 2003-10-16 N021487-002 NAMENDA MEMANTINE HYDROCHLORIDE 10MG TABLET / ORAL RLD 2003-10-16
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 N021487-001 NAMENDA 5MG TABLET / ORAL RLD 2003-10-16 a50c72e98297…2026-08-01 22:54:32 2026-06 N021487-002 NAMENDA 10MG TABLET / ORAL RLD 2003-10-16 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 · 3 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 21695-232-60 Namenda 60 in 1 BOTTLE TABLET 60 1
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21695-232 NAMENDA (MEMANTINE HYDROCHLORIDE) TABLET [REBEL DISTRIBUTORS CORP] 1 Legacy NDC, 1 package rows 20110104_74ce605d-b493-4b95-9d59-9253f81f4e20.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 21695-232-60 21695023260 60 in 1 BOTTLE Historical