43598-538 : Bupropion Hydrochloride Sr 200 mg Oral Tablet, Film Coated, Extended Release

NDC:	43598-538
Labeler:	Dr. Reddy’s Laboratories Inc.
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride Sr
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	ANDA205794
Rev. Date:	Aug 1, 2016

Appearance:

Markings:	SG;176
Shapes:	Round
Colors:	Pink
Size (mm):	12
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:

43598-538-60: 60 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (43598‑538‑60)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

200 mg

Inactive Ingredients:

Copovidone
Cysteine Hydrochloride
Hypromelloses
Magnesium Stearate
Cellulose, Microcrystalline
Polyethylene Glycols
Polysorbate 80
Titanium Dioxide
Fd&c Red No. 40

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 43598-538 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.