49884-789 : Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	49884-789
Labeler:	Par Pharmaceutical, Inc.
Product Type:	Human Prescription Drug
Drug Name:	Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA206137
Rev. Date:	Oct 26, 2016

Appearance:

Markings:	p;789
Shapes:	Round
Colors:	Orange
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:

49884-789-09: 90 BOTTLE IN 1 BOTTLE (49884‑789‑09) > 30 TABLET, FILM COATED IN 1 BOTTLE (49884‑789‑11)
49884-789-11: 30 TABLET, FILM COATED IN 1 BOTTLE (49884‑789‑11)

Active Ingredients:

Olmesartan Medoxomil
Amlodipine Besylate
Hydrochlorothiazide

Dosage Strength:

10 mg
12.5 mg
40 mg

Inactive Ingredients:

Cellulose, Microcrystalline
Starch, Pregelatinized Corn
Croscarmellose Sodium
Magnesium Stearate
Titanium Dioxide
Polyethylene Glycol 1000
Talc
Fd&c Yellow No. 6
Polyvinyl Alcohol (100000 Mw)

Pharmaceutical Classes:

Angiotensin 2 Receptor Antagonists [MoA]
Angiotensin 2 Receptor Blocker [EPC]
Calcium Channel Antagonists [MoA]
Calcium Channel Blocker [EPC]
Cytochrome P450 3A Inhibitors [MoA]
Dihydropyridine Calcium Channel Blocker [EPC]
Dihydropyridines [CS]
Increased Diuresis [PE]
Thiazide Diuretic [EPC]
Thiazides [CS]

NDC QR Code

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NDC 49884-789 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.