0093-3242 : Bisoprolol Fumarate and Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	0093-3242
Labeler:	Teva Pharmaceuticals USA, Inc.
Product Type:	Human Prescription Drug
Drug Name:	Bisoprolol Fumarate and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	NDA020186
Rev. Date:	Aug 7, 2019

Appearance:

Markings:	b;50
Shapes:	Round
Colors:	Pink
Size (mm):	7
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:

• 0093-3242-01: 100 TABLET, FILM COATED IN 1 BOTTLE (0093‑3242‑01)

Active Ingredients:

• Bisoprolol Fumarate
• Hydrochlorothiazide

Inactive Ingredients:

• Starch, Corn
• Hypromelloses
• Magnesium Stearate
• Cellulose, Microcrystalline
• Polyethylene Glycol, Unspecified
• Polysorbate 80
• Titanium Dioxide
• Ferric Oxide Yellow
• Ferric Oxide Red
• Silicon Dioxide
• Dibasic Calcium Phosphate Dihydrate /

Pharmaceutical Classes:

• Adrenergic beta-Antagonists [MoA]
• Increased Diuresis [PE]
• Thiazide Diuretic [EPC]
• Thiazides [CS]
• beta-Adrenergic Blocker [EPC]

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