Bupropion Hydrochloride 00115-6811-08

Package NDC

00115-6811-08

Manufacturer: Amneal Pharmaceuticals Of New York Llc
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 1, 2009
Listing Expires: December 31, 2026
Application: ANDA077415

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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]

Selected Package

00115-6811-08Selected

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-08)

Other packages for this product(2)

00115-6811-02

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-02)

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00115-6811-10

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-10)

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