NDC 72888-132 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72888-132

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Advagen Pharma Ltd
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077661
Marketed since
September 22, 2022
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
72888-132-001000 TABLET in 1 BOTTLE (72888-132-00)Sep 22, 2022
72888-132-01100 TABLET in 1 BOTTLE (72888-132-01)Sep 22, 2022
72888-132-05500 TABLET in 1 BOTTLE (72888-132-05)Sep 22, 2022
72888-132-3030 TABLET in 1 BOTTLE (72888-132-30)Sep 22, 2022

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