Bupropion Hydrochloride Sr 00591-3543

Generic: Bupropion Hydrochloride

Product NDC

00591-3543

Manufacturer: Actavis Pharma, Inc.
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 11, 2009
Listing Expires: December 31, 2027
Application: ANDA079094

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Active Ingredients

Ingredient	Strength
Bupropion Hydrochloride	150 mg/1

Drug Class

Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]

Packaging Options(2)

00591-3543-60

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3543-60)

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00591-3543-76

1 BOTTLE, PLASTIC in 1 CARTON (0591-3543-76) / 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

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