NDC 63629-7308 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-7308

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077662
Marketed since
April 1, 2006
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (6)

Package NDCDescriptionSince
63629-7308-190 TABLET in 1 BOTTLE (63629-7308-1)May 1, 2026
63629-7308-218 TABLET in 1 BOTTLE (63629-7308-2)May 1, 2026
63629-7308-358 TABLET in 1 BOTTLE (63629-7308-3)May 1, 2026
63629-7308-460 TABLET in 1 BOTTLE (63629-7308-4)May 1, 2026
63629-7308-530 TABLET in 1 BOTTLE (63629-7308-5)May 1, 2026
63629-7308-6120 TABLET in 1 BOTTLE (63629-7308-6)May 1, 2026

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