NDC 68180-320 – Bupropion Hydrochloride XL

Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC68180-320

Product details

Brand name
Bupropion Hydrochloride XL
Generic name
Bupropion Hydrochloride
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090693
Marketed since
June 14, 2017
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
68180-320-02500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-320-02)Jun 14, 2017
68180-320-0630 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-320-06)Jun 14, 2017
68180-320-0990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-320-09)Jun 14, 2017

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