NDC 65862-200 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC65862-200

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Aurobindo Pharma Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078787
Marketed since
January 31, 2008
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (5)

Package NDCDescriptionSince
65862-200-01100 CAPSULE in 1 BOTTLE (65862-200-01)Jan 31, 2008
65862-200-05500 CAPSULE in 1 BOTTLE (65862-200-05)Jan 31, 2008
65862-200-1010 BLISTER PACK in 1 CARTON (65862-200-10) / 10 CAPSULE in 1 BLISTER PACKJan 31, 2008
65862-200-27270 CAPSULE in 1 BOTTLE (65862-200-27)Apr 29, 2021
65862-200-9090 CAPSULE in 1 BOTTLE (65862-200-90)Apr 29, 2021

Recalls mentioning this NDC

Other Gabapentin products