NDCFind

Bupropion Hydrochloride 71209-0052-11

Package NDC

71209-0052-11

Product NDC: 71209-0052

Manufacturer
Cadila Pharmaceuticals Limited
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
January 16, 2020
Listing Expires
December 31, 2027
Application
ANDA208606
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride75 mg/1

Drug Class

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

Selected Package

71209-0052-11Selected

1000 TABLET, FILM COATED in 1 BOTTLE (71209-052-11)

Other packages for this product(2)

100 TABLET, FILM COATED in 1 BOTTLE (71209-052-05)

10 BLISTER PACK in 1 CARTON (71209-052-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK