0615-7660 : Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet

NDC:	0615-7660
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	ANDA077455
Rev. Date:	Mar 12, 2008

Appearance:

Markings:	A;133
Shapes:	Round
Colors:	Yellow
Size (mm):	11
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.

A 133: (67767-133) Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Ncs Healthcare of Ky, Inc Dba Vangard Labs

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:

0615-7660-39: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK (0615‑7660‑39)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

150 mg

Inactive Ingredients:

Copovidone K25-31
Silicon Dioxide
Hydroxypropyl Cellulose
Hypromelloses
Magnesium Stearate
Cellulose, Microcrystalline
Polydextrose
Polyethylene Glycols
Titanium Dioxide
Triacetin
Ferric Oxide Yellow

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 0615-7660 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.