NDC 68001-613 – Bupropion hydrochloride

Bupropion Hydrochloride 150 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68001-613

Product details

Brand name
Bupropion hydrochloride
Generic name
Bupropion hydrochloride
Labeler
BluePoint Laboratories
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215568
Marketed since
April 8, 2024
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
68001-613-03500 TABLET in 1 BOTTLE (68001-613-03)Apr 8, 2024
68001-613-0430 TABLET in 1 BOTTLE (68001-613-04)Jun 25, 2024
68001-613-0590 TABLET in 1 BOTTLE (68001-613-05)Jun 24, 2024

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