57664-799 : Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	57664-799
Labeler:	Sun Pharmaceutical Industries, Inc.
Product Type:	Human Prescription Drug
Drug Name:	Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	NDA200175
Rev. Date:	Oct 26, 2016

Appearance:

Markings:	C55
Shapes:	Round
Colors:	Red
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.

NDC Package Codes:

• 57664-799-83: 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (57664‑799‑83)
• 57664-799-99: 90 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (57664‑799‑99)

Active Ingredients:

• Olmesartan Medoxomil
• Amlodipine Besylate
• Hydrochlorothiazide

Pharmaceutical Classes:

• Angiotensin 2 Receptor Antagonists [MoA]
• Angiotensin 2 Receptor Blocker [EPC]
• Calcium Channel Antagonists [MoA]
• Dihydropyridine Calcium Channel Blocker [EPC]
• Dihydropyridines [Chemical/Ingredient]
• Increased Diuresis [PE]
• Thiazide Diuretic [EPC]
• Thiazides [Chemical/Ingredient]

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• 57664-798 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Sun Pharmaceutical Industries, Inc.
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