141 Pill: white, round, 8mm

The pill with imprint 141 (White, Round, 8 mm) has been identified as Bupropion Hydrochloride Extended-Release (XL) 150 mg.

It is used for Major Depressive Disorder, Depression, Seasonal Affective Disorder, and Smoking Cessation, and belongs to the drug classes miscellaneous antidepressants, smoking cessation agents, not a controlled substance.

Images for 141

Bupropion hydrochloride extended-release (XL) 150 mg 141

Bupropion Hydrochloride Extended-Release (XL)

Strength: 150 mg
Availability: Prescription only
Imprint: 141
Color: White
Shape: Round
Size: 8 mm
Drug Class: Miscellaneous antidepressants, Smoking cessation agents
Pregnancy Category: C - Risk cannot be ruled out
CSA Schedule: Not a controlled drug

Where to get medical help

Call 911 if the person has collapsed, is having a seizure, or is struggling to breathe. Otherwise call Poison Control on 1-800-222-1222 — free, 24/7. Call even if there are no symptoms: with some medicines they can be delayed. Don't try to make the person vomit.

Have ready: the imprint "141", the strength, roughly how many were taken, and when.
Pets: your vet, ASPCA Animal Poison Control on 888-426-4435, or Pet Poison Helpline on 855-764-7661 (both charge a consultation fee).
Outside the US: contact your local poison centre or emergency number.

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Previously listed products

NDC Code	Labeler	Drug Name	Generic name	Dosage form	Route	Application Number	Product Type	Approx. year
45963-141	Actavis Pharma, Inc.	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	ANDA077285	HUMAN PRESCRIPTION DRUG	2017
63739-449	McKesson Packaging Services a Business unit of McKesson Corporation	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	ANDA077285	HUMAN PRESCRIPTION DRUG	2016
67767-141	Actavis South Atlantic LLC	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	ANDA077285	HUMAN PRESCRIPTION DRUG	2015
68084-251	American Health Packaging	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	ANDA077285	HUMAN PRESCRIPTION DRUG	2015