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| Product NDC Code | 70771-1016 | ||||||||||||||
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| Drug Name | Nateglinide |
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| Type | Generic | ||||||||||||||
| Pharm Class | Glinide [EPC], Potassium Channel Antagonists [MoA] |
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| Active Ingredients |
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| Route | ORAL | ||||||||||||||
| Dosage Form | TABLET, FILM COATED | ||||||||||||||
| RxCUI drug identifier | 311919, 314142 |
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| Application Number | ANDA205248 | ||||||||||||||
| 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.Nateglinide Nateglinide NATEGLINIDE NATEGLINIDE ANHYDROUS CITRIC ACID SILICON DIOXIDE STARCH, CORN CROSPOVIDONE HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE POLYSORBATE 80 POLYETHYLENE GLYCOL, UNSPECIFIED POVIDONE TALC TITANIUM DIOXIDE WHITE TO OFF-WHITE ROUND 721 Nateglinide Nateglinide NATEGLINIDE NATEGLINIDE ANHYDROUS CITRIC ACID CROSPOVIDONE FERRIC OXIDE RED FERRIC OXIDE YELLOW HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE POLYETHYLENE GLYCOL, UNSPECIFIED POLYSORBATE 80 POVIDONE SILICON DIOXIDE STARCH, CORN TALC TITANIUM DIOXIDE LIGHT ORANGE TO ORANGE OVAL 722
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 70771-1015-9 in bottle of 90 tablets Nateglinide Tablets USP, 60 mg Rx only 90 tablets NDC 70771-1016-9 in bottle of 90 tablets Nateglinide Tablets USP, 120 mg Rx only 90 tablets nateglinide tabs 60 mg nateglinide tabs 120 mg
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