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Product NDC Code | 70771-1882 | ||||
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Drug Name | Valsartan |
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Type | Generic | ||||
Pharm Class | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC] |
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Active Ingredients |
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Route | ORAL | ||||
Dosage Form | TABLET, FILM COATED | ||||
RxCUI drug identifier | 349199, 349200, 349201, 349483 |
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Application Number | ANDA218991 | ||||
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.Valsartan Valsartan VALSARTAN VALSARTAN CROSPOVIDONE FERRIC OXIDE YELLOW HYPROMELLOSE 2910 (6 MPA.S) MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL 6000 SILICON DIOXIDE TALC TITANIUM DIOXIDE light yellow to yellow T;4 Valsartan Valsartan VALSARTAN VALSARTAN CROSPOVIDONE FERRIC OXIDE RED FERRIC OXIDE YELLOW HYPROMELLOSE 2910 (6 MPA.S) MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL 6000 SILICON DIOXIDE TALC TITANIUM DIOXIDE light pink to pink T7 Valsartan Valsartan VALSARTAN VALSARTAN CROSPOVIDONE FERRIC OXIDE YELLOW HYPROMELLOSE 2910 (6 MPA.S) MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL 6000 SILICON DIOXIDE TALC TITANIUM DIOXIDE light yellow to yellow 277 Valsartan Valsartan VALSARTAN VALSARTAN CROSPOVIDONE FERRIC OXIDE RED FERRIC OXIDE YELLOW FERROSOFERRIC OXIDE HYPROMELLOSE 2910 (6 MPA.S) MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL 6000 SILICON DIOXIDE TALC TITANIUM DIOXIDE light brown to brown 278
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 Valsartan tablets USP, 40 mg NDC 70771-1882-3 Bottle of 30 Scored Tablets Rx only Valsartan tablets USP, 80 mg NDC 70771-1883-9 Bottle of 90 tablets Rx only Valsartan tablets USP, 160 mg NDC 70771-1884-9 Bottle of 90 tablets Rx only Valsartan tablets USP, 320 mg NDC 70771-1885-9 Bottle of 90 tablets Rx only 40 mg 80 mg 160 mg 320 mg
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.SPL UNCLASSIFIED
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