NDC 70436-060 – Bupropion Hydrochloride SR

Bupropion Hydrochloride 200 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC70436-060

Product details

Brand name
Bupropion Hydrochloride SR
Generic name
Bupropion hydrochloride
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211347
Marketed since
November 2, 2020
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
70436-060-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-060-01)Nov 2, 2020
70436-060-02500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-060-02)Nov 2, 2020
70436-060-0560 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-060-05)Nov 2, 2020

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