Olmesartan Medoxomil And Amlodipine Besylate And Hydrochlorothiazide 70436-0017

Product NDC

70436-0017

Manufacturer: Slate Run Pharmaceuticals, Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 15, 2025
Listing Expires: December 31, 2026
Application: ANDA210718

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Active Ingredients

Ingredient	Strength
Amlodipine Besylate	10 mg/1
Hydrochlorothiazide	12.5 mg/1
Olmesartan Medoxomil	40 mg/1

Drug Class

Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]

Packaging Options(2)

70436-0017-04

30 TABLET, FILM COATED in 1 BOTTLE (70436-017-04)

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70436-0017-06

90 TABLET, FILM COATED in 1 BOTTLE (70436-017-06)

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