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| Product NDC Code | 70771-1075 | ||||||||||||||
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| Drug Name | Budesonide |
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| Type | Generic | ||||||||||||||
| Pharm Class | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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| Active Ingredients |
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| Route | ORAL | ||||||||||||||
| Dosage Form | CAPSULE, COATED PELLETS | ||||||||||||||
| RxCUI drug identifier | 1244214 | ||||||||||||||
| Application Number | ANDA206134 | ||||||||||||||
| 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.budesonide budesonide BUDESONIDE BUDESONIDE ACETYLTRIBUTYL CITRATE ALCOHOL AMMONIA BUTYL ALCOHOL DIMETHICONE ETHYLCELLULOSES FERRIC OXIDE RED FERRIC OXIDE YELLOW FERROSOFERRIC OXIDE GELATIN ISOPROPYL ALCOHOL METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER POLYSORBATE 80 POTASSIUM HYDROXIDE PROPYLENE GLYCOL SHELLAC SODIUM LAURYL SULFATE SUCROSE TALC TITANIUM DIOXIDE TRIETHYL CITRATE WATER OPAQUE LIGHT-ORANGE OPAQUE WHITE CAPSULE 720
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 70771-1075-1 in bottle of 100 capsules Budesonide Delayed-Release Capsules (Enteric Coated) 3 mg 100 capsules Rx only Budesonide Capsules 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