71335-1044 : Bupropion Hydrochloride 150 mg Oral Tablet, Extended Release

NDC:	71335-1044
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA210497
Rev. Date:	Nov 8, 2018

Appearance:

Markings:	GS1
Shapes:	Round
Colors:	White
Size (mm):	7
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

71335-1044-1: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71335‑1044‑1)
71335-1044-2: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71335‑1044‑2)
71335-1044-3: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71335‑1044‑3)
71335-1044-4: 120 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71335‑1044‑4)
71335-1044-5: 14 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71335‑1044‑5)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

150 mg

Inactive Ingredients:

Povidone K90
Cysteine Hydrochloride
Silicon Dioxide
Glyceryl Dibehenate
Magnesium Stearate
Ethylcellulose, Unspecified
Polyethylene Glycol 1450
Hydrated Silica
Triethyl Citrate
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Shellac
Ferrosoferric Oxide
Propylene Glycol /

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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NDC 71335-1044 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.