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| Product NDC Code | 70771-1369 | ||||||
|---|---|---|---|---|---|---|---|
| Drug Name | Chlorthalidone |
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| Type | Generic | ||||||
| Pharm Class | Increased Diuresis [PE], Thiazide-like Diuretic [EPC] |
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| Active Ingredients |
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| Route | ORAL | ||||||
| Dosage Form | TABLET | ||||||
| RxCUI drug identifier | 197499, 197500 |
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| Application Number | ANDA207813 | ||||||
| Labeler Name | Zydus Lifesciences Limited | ||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Spl product data elements
Usually a list of ingredients in a drug product.Chlorthalidone Chlorthalidone CHLORTHALIDONE CHLORTHALIDONE CELLULOSE, MICROCRYSTALLINE FERRIC OXIDE YELLOW SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN STEARIC ACID LIGHT YELLOW ROUND Z25 Chlorthalidone Chlorthalidone CHLORTHALIDONE CHLORTHALIDONE CELLULOSE, MICROCRYSTALLINE SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN STEARIC ACID WHITE ROUND Z;50
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1369-1 Chlorthalidone tablets USP ,25 mg Rx only 100 tablets NDC 70771-1370-1 Chlorthalidone tablets USP, 50 mg Rx only 100 tablets Chlorthalidone tablets, USP Chlorthalidone tablets, USP
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API