NDC 65862-326 – Donepezil Hydrochloride

Donepezil Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-326

Product details

Brand name
Donepezil Hydrochloride
Generic name
Donepezil Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090056
Marketed since
May 31, 2011
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Donepezil Hydrochloride →

Package NDC codes (6)

Package NDCDescriptionSince
65862-326-01100 TABLET, FILM COATED in 1 BOTTLE (65862-326-01)May 31, 2011
65862-326-05500 TABLET, FILM COATED in 1 BOTTLE (65862-326-05)May 31, 2011
65862-326-1410 BLISTER PACK in 1 CARTON (65862-326-14) / 14 TABLET, FILM COATED in 1 BLISTER PACKMay 31, 2011
65862-326-3030 TABLET, FILM COATED in 1 BOTTLE (65862-326-30)May 31, 2011
65862-326-9090 TABLET, FILM COATED in 1 BOTTLE (65862-326-90)May 31, 2011
65862-326-991000 TABLET, FILM COATED in 1 BOTTLE (65862-326-99)May 31, 2011

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