NDC 82804-015 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-015

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
April 11, 2016
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (3)

Package NDCDescriptionSince
82804-015-3030 TABLET in 1 BOTTLE (82804-015-30)Oct 3, 2023
82804-015-6060 TABLET in 1 BOTTLE (82804-015-60)Oct 3, 2023
82804-015-9090 TABLET in 1 BOTTLE (82804-015-90)Oct 3, 2023

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