Memantine Hydrochloride

Product NDC
72606-514
11-digit product format
726060514
Labeler code
72606
Product ID
72606-514_c46fb7ce-bb2c-48ef-84ac-9da1a7fec412
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Memantine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
CELLTRION USA, INC.
Application
ANDA090073
Marketing category
ANDA
Marketing start
2020-06-05
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
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
94db636e-a074-45fd-8e8d-331920a99436Product name420250103
941773f8-a40e-0684-da08-ff9a143e6368Product name720231219
5b597f00-4538-4686-aa4e-3c60ed3788c8Product name220210511
1836e79a-a4d1-4087-2f2e-f878e8a1fef2Product name920151209

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72606-514-02EA - Each72606-5142022fd45-b795-49c6-b1db-ec47c25c3e8c12020-09-14
72606-514-04EA - Each72606-5141fdd8c6b-7b6b-4454-8035-b9913cf95e7312020-09-14

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
996571memantine HCl 5 MG Oral TabletPSNd77172c4-f84a-4310-907f-7222d330a383100
996571memantine hydrochloride 5 MG Oral TabletSCDd77172c4-f84a-4310-907f-7222d330a383100

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
72606-514-027260605140260 TABLET, FILM COATED in 1 BOTTLE (72606-514-02) 2020-06-050000-00-00NoNoCurrent
72606-514-0472606051404500 TABLET, FILM COATED in 1 BOTTLE (72606-514-04) 2020-06-050000-00-00NoNoCurrent