NDC 65862-523 – Gabapentin

Gabapentin 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-523

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200651
Marketed since
October 6, 2011
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
65862-523-01100 TABLET, FILM COATED in 1 BOTTLE (65862-523-01)Oct 6, 2011
65862-523-05500 TABLET, FILM COATED in 1 BOTTLE (65862-523-05)Oct 6, 2011
65862-523-262500 TABLET, FILM COATED in 1 BOTTLE (65862-523-26)Oct 6, 2011
65862-523-9090 TABLET, FILM COATED in 1 BOTTLE (65862-523-90)Oct 6, 2011

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