NDC 82804-193 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-193

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
October 1, 2021
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
82804-193-3030 TABLET in 1 BOTTLE (82804-193-30)Apr 16, 2025
82804-193-9090 TABLET in 1 BOTTLE (82804-193-90)Feb 7, 2025

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