Candesartan Cilexetil And Hydrochlorothiazide Tablet
FDA Label NDC 70771-1325

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zydus Lifesciences Limited for the product Candesartan Cilexetil And Hydrochlorothiazide (NDC 70771-1325). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Package Label.Principal Display Panel

NDC 70771-1325-0 in bottle of 1000 tablets

Candesartan Cilexetil and Hydrochlorothiazide Tablets USP, 16 mg/12.5 mg

Rx only

1000 tablets

Candesartan Cilexetil And Hydrochlorothiazide  Tablets (63e427ec 872d 47c2 9510 F419b21580d8 03)

Candesartan Cilexetil And Hydrochlorothiazide Tablets (63e427ec 872d 47c2 9510 F419b21580d8 03)

NDC 70771-1326-0 in bottle of 1000 tablets

Candesartan Cilexetil and Hydrochlorothiazide Tablets USP, 32 mg/12.5 mg

Rx only

1000 tablets

Candesartan Cilexetil And Hydrochlorothiazide  Tablets (63e427ec 872d 47c2 9510 F419b21580d8 04)

Candesartan Cilexetil And Hydrochlorothiazide Tablets (63e427ec 872d 47c2 9510 F419b21580d8 04)

NDC 70771-1327-0 in bottle of 1000 tablets

Candesartan Cilexetil and Hydrochlorothiazide Tablets USP, 32 mg/25 mg

Rx only

1000 tablets

Candesartan Cilexetil And Hydrochlorothiazide  Tablets (63e427ec 872d 47c2 9510 F419b21580d8 05)

Candesartan Cilexetil And Hydrochlorothiazide Tablets (63e427ec 872d 47c2 9510 F419b21580d8 05)

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