NDC 42806-415 – Bupropion Hydrochloride

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

Human Prescription Drug

Product NDC42806-415

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Epic Pharma LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA075932
Marketed since
December 15, 2021
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
42806-415-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-01)Dec 15, 2021
42806-415-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-05)Dec 15, 2021
42806-415-52250 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-52)Dec 15, 2021
42806-415-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-60)Dec 15, 2021

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