70518-2029 : Bupropion Hydrochloride Sr 100 mg Oral Tablet, Film Coated, Extended Release

NDC:	70518-2029
Labeler:	Remedyrepack Inc.
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride Sr
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	ANDA079095
Rev. Date:	Apr 18, 2019

Appearance:

Markings:	WPI;858
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.

WPI 858: (0591-3540) Bupropion Hydrochloride Sr 100 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

70518-2029-0: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK (70518‑2029‑0)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

100 mg

Inactive Ingredients:

Hydroxypropyl Cellulose (1600000 Wamw)
Cellulose, Microcrystalline
Silicon Dioxide
Stearic Acid
Magnesium Stearate
Hydrochloric Acid
Lactose Monohydrate
Titanium Dioxide
Polyethylene Glycol, Unspecified /

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 70518-2029 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.