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Product NDC Code | 65841-705 | ||||||||
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Drug Name | Gabapentin |
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Type | Generic | ||||||||
Pharm Class | Decreased Central Nervous System Disorganized Electrical Activity [PE] | ||||||||
Active Ingredients |
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Route | ORAL | ||||||||
Dosage Form | TABLET, FILM COATED | ||||||||
Application Number | ANDA078926 | ||||||||
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.Gabapentin Gabapentin GABAPENTIN GABAPENTIN COPOVIDONE K25-31 HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED MAGNESIUM STEARATE MANNITOL POLOXAMER 407 POVIDONE TALC WHITE TO OFF-WHITE OVAL ZE72 Gabapentin Gabapentin GABAPENTIN GABAPENTIN COPOVIDONE K25-31 HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED MAGNESIUM STEARATE MANNITOL POLOXAMER 407 POVIDONE TALC WHITE TO OFF-WHITE OVAL ZE71
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 65841-705-01 in bottle of 100 tablets Gabapentin Tablets USP, 600 mg R x only 100 tablets NDC 65841-706-01 in bottle of 100 tablets Gabapentin Tablets USP, 800 mg R x only 100 tablets Gabapentin tablets Gabapentin tablets
Spl medguide
Information about the patient medication guide that accompanies the drug product. Certain drugs must be dispensed with an accompanying medication guide. This field may contain information about when to consult the medication guide and the contents of the medication guide.Manufactured by: Cadila Heathcare Ltd. India
SPL MEDGUIDE
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