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| Product NDC Code | 70771-1512 | ||||||
|---|---|---|---|---|---|---|---|
| Drug Name | Albuterol |
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| Type | Generic | ||||||
| Pharm Class | Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC] |
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| Active Ingredients |
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| Route | ORAL | ||||||
| Dosage Form | TABLET | ||||||
| RxCUI drug identifier | 197316, 197318 |
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| Application Number | ANDA208884 | ||||||
| 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.Albuterol Albuterol ALBUTEROL SULFATE ALBUTEROL LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POVIDONE K30 SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN white to off-white ROUND 10;61 Albuterol Albuterol ALBUTEROL SULFATE ALBUTEROL LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POVIDONE K30 SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN WHITE TO OFF-WHITE ROUND 10;62
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 70771-1511-1 in bottle of 100 tablets Albuterol tablets USP, 2 mg Rx only 100 Tablets NDC 70771-1512-1 in bottle of 100 tablets Albuterol tablets USP, 4 mg Rx only 100 Tablets label 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