NDC 68382-607 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-607

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203934
Marketed since
January 25, 2024
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (3)

Package NDCDescriptionSince
68382-607-05500 TABLET in 1 BOTTLE (68382-607-05)Jan 25, 2024
68382-607-1690 TABLET in 1 BOTTLE (68382-607-16)Jan 25, 2024
68382-607-7710 BLISTER PACK in 1 CARTON (68382-607-77) / 10 TABLET in 1 BLISTER PACK (68382-607-30)Jan 25, 2024

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