NDC 72789-217 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-217

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
February 4, 2016
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
72789-217-6060 TABLET in 1 BOTTLE, PLASTIC (72789-217-60)Nov 19, 2021

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