33342-173 : Olmesartan Medoxomil and Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	33342-173
Labeler:	Macleods Pharmaceuticals Limited
Product Type:	Human Prescription Drug
Drug Name:	Olmesartan Medoxomil and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA204801
Rev. Date:	Jun 2, 2023

NDC Package Codes:

33342-173-07: 30 TABLET, FILM COATED IN 1 BOTTLE (33342‑173‑07)
33342-173-10: 90 TABLET, FILM COATED IN 1 BOTTLE (33342‑173‑10)
33342-173-12: 10 BLISTER PACK IN 1 CARTON (33342‑173‑12) / 10 TABLET, FILM COATED IN 1 BLISTER PACK
33342-173-44: 1000 TABLET, FILM COATED IN 1 BOTTLE (33342‑173‑44)

Active Ingredients:

Hydrochlorothiazide
Olmesartan Medoxomil

Dosage Strength:

12.5 mg
20 mg

Pharmaceutical Classes:

Angiotensin 2 Receptor Antagonists [MoA]
Angiotensin 2 Receptor Blocker [EPC]
Increased Diuresis [PE]
Thiazide Diuretic [EPC]
Thiazides [CS]

NDC QR Code

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NDC 33342-173 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.