NDC 65862-199 – Gabapentin

Gabapentin 300 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC65862-199

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 (9)

Package NDCDescriptionSince
65862-199-01100 CAPSULE in 1 BOTTLE (65862-199-01)Jan 31, 2008
65862-199-05500 CAPSULE in 1 BOTTLE (65862-199-05)Jan 31, 2008
65862-199-1010 BLISTER PACK in 1 CARTON (65862-199-10) / 10 CAPSULE in 1 BLISTER PACKJan 31, 2008
65862-199-18180 CAPSULE in 1 BOTTLE (65862-199-18)Apr 29, 2021
65862-199-27270 CAPSULE in 1 BOTTLE (65862-199-27)Apr 29, 2021
65862-199-3030 CAPSULE in 1 BOTTLE (65862-199-30)Apr 29, 2021
65862-199-6060 CAPSULE in 1 BOTTLE (65862-199-60)Apr 29, 2021
65862-199-9090 CAPSULE in 1 BOTTLE (65862-199-90)Apr 29, 2021
65862-199-991000 CAPSULE in 1 BOTTLE (65862-199-99)Jan 31, 2008

Recalls mentioning this NDC

Other Gabapentin products