NDC 69097-811 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69097-811

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Cipla USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202764
Marketed since
July 22, 2016
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (3)

Package NDCDescriptionSince
69097-811-0230 TABLET in 1 BOTTLE (69097-811-02)Jul 22, 2016
69097-811-07100 TABLET in 1 BOTTLE (69097-811-07)Jul 22, 2016
69097-811-12500 TABLET in 1 BOTTLE (69097-811-12)Jul 22, 2016

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