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Gabapentin - Medication Information

Product NDC Code 68071-4784
Drug Name

Gabapentin

Type Generic
Pharm Class Decreased Central Nervous System Disorganized Electrical Activity [PE]
Active Ingredients
Gabapentin 300 mg/1
Route ORAL
Dosage Form CAPSULE
RxCUI drug identifier 310431
Application Number ANDA090007
Labeler Name NuCare Pharmaceuticals,Inc.
Packages
Package NDC Code Description
68071-4784-1 100 capsule in 1 bottle (68071-4784-1)
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Spl product data elements

Usually a list of ingredients in a drug product.
GABAPENTIN GABAPENTIN LACTOSE MONOHYDRATE STARCH, CORN TALC GELATIN TITANIUM DIOXIDE FERRIC OXIDE YELLOW PROPYLENE GLYCOL SHELLAC GABAPENTIN GABAPENTIN 104

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.
pdp

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.
gab medguide

How supplied

Information about the available dosage forms to which the labeling applies, and for which the manufacturer or distributor is responsible. This field ordinarily includes the strength of the dosage form (in metric units), the units in which the dosage form is available for prescribing, appropriate information to facilitate identification of the dosage forms (such as shape, color, coating, scoring, and National Drug Code), and special handling and storage condition information.
HOW SUPPLIED 100 mg Capsules (White/White colored, size 3 hard gelatin capsules with 103 printed on body of capsules containing white to off white granular powder) NDC 68071-4784-1 BOTTLES OF 100

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