71765-002 : Bupropion Hydrochloride XL 300 mg Oral Tablet, Extended Release

NDC:	71765-002
Labeler:	Zhejiang Jutai Pharamceutical Co., Ltd
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride XL
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA211200
Rev. Date:	Sep 6, 2019

Appearance:

Markings:	T011
Shapes:	Round
Colors:	White
Size (mm):	10
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:

71765-002-03: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71765‑002‑03)
71765-002-09: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71765‑002‑09)
71765-002-50: 500 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71765‑002‑50)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

300 mg

Inactive Ingredients:

Alcohol
Ethylcellulose, Unspecified
Hydrochloric Acid
Hydroxypropyl Cellulose, Unspecified
Hypromellose, Unspecified
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Polyethylene Glycol, Unspecified
Povidone, Unspecified
Silicon Dioxide
Stearic Acid
Talc
Ferrosoferric Oxide
Propylene Glycol
Water /

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 71765-002 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.