NDC 68001-412 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68001-412

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
BluePoint Laboratories
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077662
Marketed since
September 30, 2019
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
68001-412-00100 TABLET in 1 BOTTLE (68001-412-00)Sep 30, 2019
68001-412-03500 TABLET in 1 BOTTLE (68001-412-03)Sep 30, 2019

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