Memantine Hydrochloride

Product NDC
64679-122
11-digit product format
646790122
Labeler code
64679
Product ID
64679-122_2377358b-8cd4-4446-9a83-83c05986fa74
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Memantine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Wockhardt USA LLC.
Application
ANDA090073
Marketing category
ANDA
Marketing start
2015-09-04
Marketing end
0000-00-00
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
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64679-122-02EA - Each64679-1229b2640aa-53eb-4d9a-a08c-5a706b536a3312015-12-02
64679-122-03EA - Each64679-12292d74450-3eca-46d6-97c5-4208dc944f0012015-12-02