NDC 69238-1552 – Memantine and Donepezil Hydrochlorides Extended-release

Memantine Hydrochloride 7 mg/1; Donepezil Hydrochloride 10 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC69238-1552

Product details

Brand name
Memantine and Donepezil Hydrochlorides Extended-release
Generic name
Memantine and Donepezil
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA208328
Marketed since
February 1, 2017
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor; N-methyl-D-aspartate Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Memantine and Donepezil Hydrochlorides Extended-release →

Package NDC codes (2)

Package NDCDescriptionSince
69238-1552-330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69238-1552-3)Feb 1, 2017
69238-1552-990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69238-1552-9)Feb 1, 2017

Other Memantine and Donepezil Hydrochlorides Extended-release products