donepezil hydrochloride

Product NDC: 68071-1523
11-digit product format: 680711523
Labeler code: 68071
Product ID: 68071-1523_d5d067d8-3e69-66a9-e053-2995a90a6ece
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: donepezil hydrochloride
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: NuCare Pharmaceuticals,Inc.
Application: ANDA200292
Marketing category: ANDA
Marketing start: 2011-11-01
Marketing end: 0000-00-00
Substance: DONEPEZIL HYDROCHLORIDE
Active strength: 10 mg/1
Pharmacologic classes: Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68071-1523-3	2020-09-18	C162847	48780-1	9d75b9d1-0f93-f424-e053-dadaa90a57ce	549e48a5-be62-0042-e054-00144ff8d46c
68071-1523-3	2020-01-31	C162847	48780-1	9d75b9d1-0f93-f424-e053-dadaa90a57ce	549e48a5-be62-0042-e054-00144ff8d46c

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
68071-1523-3	EA - Each	68071-1523	26829d81-45fb-43fd-9459-9791b2edbb99	1	2017-08-11

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3O2T2PJ89D	DONEPEZIL HYDROCHLORIDE	120011-70-3	DONEPEZIL HYDROCHLORIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
68071-1523-3	68071152303	30 TABLET, FILM COATED in 1 BOTTLE (68071-1523-3)	2017-07-18	0000-00-00	No	No	Current