71335-1866 : Bupropion Hydrochloride Sr 100 mg Oral Tablet, Film Coated, Extended Release

NDC:	71335-1866
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride Sr
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	ANDA205794
Rev. Date:	Apr 20, 2018

NDC Package Codes:

71335-1866-1: 60 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (71335‑1866‑1)
71335-1866-2: 90 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (71335‑1866‑2)
71335-1866-3: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (71335‑1866‑3)
71335-1866-4: 45 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (71335‑1866‑4)
71335-1866-5: 28 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (71335‑1866‑5)
71335-1866-6: 120 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (71335‑1866‑6)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

100 mg

Pharmaceutical Classes:

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

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.