NDC 73352-231 – Gabapentin

Gabapentin 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC73352-231

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Trifluent Pharma, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204989
Marketed since
August 17, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
73352-231-01100 CAPSULE in 1 BOTTLE, PLASTIC (73352-231-01)Aug 17, 2026

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