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| Product NDC Code | 70771-1726 | ||||||
|---|---|---|---|---|---|---|---|
| Drug Name | Bisoprolol fumarate |
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| Type | Generic | ||||||
| Pharm Class | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
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| Active Ingredients |
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| Route | ORAL | ||||||
| Dosage Form | TABLET, FILM COATED | ||||||
| RxCUI drug identifier | 854901, 854905 |
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| Application Number | ANDA215680 | ||||||
| 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.Bisoprolol Fumarate Bisoprolol Fumarate BISOPROLOL FUMARATE BISOPROLOL ALUMINUM OXIDE ANHYDROUS DIBASIC CALCIUM PHOSPHATE BUTYLATED HYDROXYANISOLE CROSPOVIDONE (12 MPA.S AT 5%) D&C YELLOW NO. 10 ALUMINUM LAKE FD&C RED NO. 40 HYPROMELLOSE 2910 (6 MPA.S) MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL 6000 SILICON DIOXIDE TITANIUM DIOXIDE light pink to pink 111 Bisoprolol Fumarate Bisoprolol Fumarate BISOPROLOL FUMARATE BISOPROLOL ANHYDROUS DIBASIC CALCIUM PHOSPHATE BUTYLATED HYDROXYANISOLE CROSPOVIDONE (12 MPA.S AT 5%) HYPROMELLOSE 2910 (6 MPA.S) MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL 6000 SILICON DIOXIDE TITANIUM DIOXIDE white to off white colored with occasional greyish 112
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 70771-1726-3 Bisoprolol Fumarate Tablets USP, 5 mg 30 Tablets Unit-of-Use Rx only NDC 70771-1727-3 Bisoprolol Fumarate Tablets USP, 10 mg 30 Tablets Unit-of-Use Rx only 5 mg label 10 mg 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