Gabapentin Capsule
FDA Label NDC 70518-2919

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Remedyrepack Inc. for the product Gabapentin (NDC 70518-2919). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding spl medguide, how supplied, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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) Bottles of 100, 500 & 1000

300 mg Capsules (Yellow/Yellow colored, size '1' hard gelatin capsules with "104" printed on body of capsules containing white to off white granular powder) Bottles of 100, 500 & 1000

400 mg Capsules (Orange/Orange colored, size '0' hard gelatin capsules with "105" printed on body of capsules containing white to off white granular powder)

NDC: 70518-2919-00

PACKAGING: 30 in 1 BLISTER PACK

Repackaged and Distributed By:

Remedy Repack, Inc.

625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

Principal Display Panel

DRUG: GABAPENTIN

GENERIC: GABAPENTIN

DOSAGE: CAPSULE

ADMINSTRATION: ORAL

NDC: 70518-2919-0

COLOR: orange

SHAPE: CAPSULE

SCORE: No score

SIZE: 21 mm

IMPRINT: 105

PACKAGING: 30 in 1 BLISTER PACK

ACTIVE INGREDIENT(S):

  • GABAPENTIN 400mg in 1
  • INACTIVE INGREDIENT(S):

    • LACTOSE MONOHYDRATE
    • STARCH, CORN
    • TALC
    • GELATIN
    • TITANIUM DIOXIDE
    • FERRIC OXIDE YELLOW
    • FD&C BLUE NO. 2
    • PROPYLENE GLYCOL
    • SHELLAC
    • Remedy_label (Remedy Label)

      Remedy_label (Remedy Label)

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