NDC 71610-778 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-778

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
November 3, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
71610-778-4545 TABLET in 1 BOTTLE (71610-778-45)Jan 25, 2024
71610-778-5360 TABLET in 1 BOTTLE (71610-778-53)Jan 31, 2024
71610-778-70120 TABLET in 1 BOTTLE (71610-778-70)Jan 25, 2024
71610-778-92270 TABLET in 1 BOTTLE (71610-778-92)Jan 25, 2024

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