0615-7864 : Bupropion Hydrochloride 75 mg Oral Tablet, Film Coated

NDC:	0615-7864
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Bupropion Hydrochloride
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA076143
Rev. Date:	Jan 17, 2006

Appearance:

Markings:	APO;BU;75
Shapes:	Round
Colors:	Orange
Size (mm):	8
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.

APO BU 75: (55154-8180) Bupropion Hydrochloride 75 mg Oral Tablet, Film Coated 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:

0615-7864-39: 30 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑7864‑39)

Active Ingredients:

Bupropion Hydrochloride

Dosage Strength:

75 mg

Inactive Ingredients:

Silicon Dioxide
Crospovidone
Fd&c Yellow No. 6
Fumaric Acid
Hydroxypropyl Cellulose (Type H)
Hypromelloses
Magnesium Stearate
Methylcellulose (100 Mpa.s)
Polyethylene Glycols
Titanium Dioxide

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 0615-7864 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.