NDC 68788-7786 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC68788-7786

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210497
Marketed since
October 21, 2020
Listing expires
December 31, 2027
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
68788-7786-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-1)Oct 21, 2020
68788-7786-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-3)Oct 21, 2020
68788-7786-660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-6)Oct 21, 2020
68788-7786-8120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-8)Oct 21, 2020
68788-7786-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-9)Oct 21, 2020

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