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717 (Hydrochlorothiazide and losartan potassium 12.5 mg / 50 mg)

Pill imprint 717 has been identified as Hydrochlorothiazide and losartan potassium 12.5 mg / 50 mg.

Hydrochlorothiazide/losartan is used in the treatment of high blood pressure and belongs to the drug class angiotensin II inhibitors with thiazides. There is positive evidence of human fetal risk during pregnancy. Hydrochlorothiazide/losartan 12.5 mg / 50 mg is not a controlled substance under the Controlled Substance Act (CSA).

Hydrochlorothiazide and losartan potassium 12.5 mg / 50 mg 717
Hydrochlorothiazide and losartan potassium 12.5 mg / 50 mg 717
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Hydrochlorothiazide and losartan potassium
Imprint:
717
Strength:
12.5 mg / 50 mg
Color:
Yellow
Shape:
Elliptical / Oval
Availability:
Prescription only
Drug Class:
Angiotensin II inhibitors with thiazides
Pregnancy Category:
D - Positive evidence of risk
CSA Schedule:
Not a controlled drug
Manufacturer:
Sandoz Inc.
National Drug Code (NDC):
00781-5816
Inactive Ingredients:
microcrystalline cellulose
lactose monohydrate
corn starch
magnesium stearate
hydroxypropyl cellulose
hypromellose
titanium dioxide
D&C Yellow No. 10
carnauba wax
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
00006-0717 Merck & Co., Inc.
54868-3866 Physicians Total Care Inc (repackager)
54569-4722 A-S Medication Solutions, LLC (repackager)
35356-0416 Lake Erie Medical and Surgical Supply (repackager)
68071-0787 Nucare Pharmaceuticals Inc (repackager)

Note: Inactive ingredients may vary.

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