Memantine Hydrochloride

Product NDC
42292-006
11-digit product format
422920006
Labeler code
42292
Product ID
42292-006_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
2015-07-31
Marketing end
2019-10-31
Substance
MEMANTINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
NMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42292-006-01EA - Each42292-00610db1ac4-5939-44b0-a9b9-e35f606f3bfa12015-09-10
42292-006-06EA - Each42292-00618fac7c0-565c-4ffa-932a-386060ef261c12015-09-10