NDC 68084-708 – BuPROPion Hydrochloride

Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC68084-708

Product details

Brand name
BuPROPion Hydrochloride
Generic name
Bupropion hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA079095
Marketed since
April 1, 2015
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

Uses, dosage, side effects and warnings for Bupropion hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
68084-708-2530 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-708-25) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-708-95)Apr 1, 2015

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