Memantine Hydrochloride

Product NDC
42292-005
11-digit product format
422920005
Labeler code
42292
Product ID
42292-005_7cef9597-5846-339f-e053-2991aa0a1efb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
memantine
Dosage form
TABLET
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA079225
Marketing category
ANDA
Marketing start
2015-08-24
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42292-005-01EA - Each42292-005fd057fe1-2d94-4bd2-ae4f-775b9d4901c212015-09-10
42292-005-06EA - Each42292-00530039fd2-5c74-4895-80eb-85af1793781c12015-09-10