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NDC 60505-4766-06 APO-VARENICLINE 1 mg/1 Details

APO-VARENICLINE 1 mg/1

APO-VARENICLINE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Apotex Corp. The primary component is VARENICLINE TARTRATE.

MedlinePlus Drug Summary

Varenicline is used along with education and counseling to help people stop smoking. Varenicline is in a class of medications called smoking cessation aids. It works by blocking the pleasant effects of nicotine (from smoking) on the brain.

Related Packages: 60505-4766-06
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Varenicline

Product Information

NDC	60505-4766
Product ID	60505-4766_cd7db833-6a04-3e59-5432-326867309b61
Associated GPIs	62100080200330
GCN Sequence Number	060897
GCN Sequence Number Description	varenicline tartrate TABLET 1 MG ORAL
HIC3	J3C
HIC3 Description	SMOKING DETERRENT-NICOTINIC RECEPT.PARTIAL AGONIST
GCN	27047
HICL Sequence Number	033766
HICL Sequence Number Description	VARENICLINE TARTRATE
Brand/Generic	Generic
Proprietary Name	APO-VARENICLINE
Proprietary Name Suffix	n/a
Non-Proprietary Name	VARENICLINE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	1
Active Ingredient Units	mg/1
Substance Name	VARENICLINE TARTRATE
Labeler Name	Apotex Corp
Pharmaceutical Class	Cholinergic Agonists [MoA], Cholinergic Receptor Agonist [EPC], Partial Cholinergic Nicotinic Agonist [EPC], Partial Cholinergic Nicotinic Agonists [MoA]
DEA Schedule	n/a
Marketing Category	UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Application Number	n/a
Listing Certified Through	n/a

Package

NDC 60505-4766-06 (60505476606)

Pricing Information	N/A
NDC Package Code	60505-4766-6
Billing NDC	60505476606
Package	56 TABLET, FILM COATED in 1 BOTTLE (60505-4766-6)
Marketing Start Date	2021-07-16
NDC Exclude Flag	N