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| Product NDC Code | 70771-1764 | ||||||
|---|---|---|---|---|---|---|---|
| Drug Name | Lubiprostone |
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| Type | Generic | ||||||
| Pharm Class | Chloride Channel Activator [EPC], Chloride Channel Activators [MoA] |
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| Active Ingredients |
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| Route | ORAL | ||||||
| Dosage Form | CAPSULE | ||||||
| RxCUI drug identifier | 616578, 794639 |
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| Application Number | ANDA214131 | ||||||
| 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.Lubiprostone Lubiprostone LUBIPROSTONE LUBIPROSTONE 1,4-SORBITAN FERRIC OXIDE RED FERROSOFERRIC OXIDE GELATIN, UNSPECIFIED MEDIUM-CHAIN TRIGLYCERIDES PROPYLENE GLYCOL SHELLAC SORBITOL TITANIUM DIOXIDE WATER light pink to pink colored 8 Lubiprostone Lubiprostone LUBIPROSTONE LUBIPROSTONE 1,4-SORBITAN FERROSOFERRIC OXIDE GELATIN, UNSPECIFIED MEDIUM-CHAIN TRIGLYCERIDES PROPYLENE GLYCOL SHELLAC SORBITOL WATER light yellow colored 24
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 70771-1763-6 Lubiprostone Capsules, 8 mcg 60 Capsules Rx only NDC 70771-1764-6 Lubiprostone Capsules, 24 mcg 60 Capsules Rx only 8 mcg label 24 mcg label
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