Bupropion Hydrochloride 72189-0124

Product NDC

72189-0124

Manufacturer: Direct Rx
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 14, 2020
Listing Expires: December 31, 2026
Application: ANDA210497

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Active Ingredients

Ingredient	Strength
Bupropion Hydrochloride	300 mg/1

Drug Class

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

Packaging Options(2)

72189-0124-30

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-124-30)

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72189-0124-72

120 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-124-72)

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