FDA Label for Candesartan Cilexetil And Hydrochlorothiazide
View Indications, Usage & Precautions
Candesartan Cilexetil And Hydrochlorothiazide Product Label
The following document was submitted to the FDA by the labeler of this product Zydus Lifesciences Limited. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
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
NDC 70771-1326-0 in bottle of 1000 tablets
Candesartan Cilexetil and Hydrochlorothiazide Tablets USP, 32 mg/12.5 mg
Rx only
1000 tablets
NDC 70771-1327-0 in bottle of 1000 tablets
Candesartan Cilexetil and Hydrochlorothiazide Tablets USP, 32 mg/25 mg
Rx only
1000 tablets
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