NDC 81033-123 – Gabapentin

Gabapentin 50 mg/mL · Solution · Oral

Human Prescription Drug

Product NDC81033-123

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Kesin Pharma Corporation
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA091286
Marketed since
August 6, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
81033-123-16473 mL in 1 BOTTLE (81033-123-16)Sep 1, 2025
81033-123-4440 CUP, UNIT-DOSE in 1 CARTON (81033-123-44) / 5 mL in 1 CUP, UNIT-DOSE (81033-123-05)Sep 1, 2025

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