NDC 65862-198 – Gabapentin

Gabapentin 100 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC65862-198

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 (7)

Package NDCDescriptionSince
65862-198-01100 CAPSULE in 1 BOTTLE (65862-198-01)Jan 31, 2008
65862-198-05500 CAPSULE in 1 BOTTLE (65862-198-05)Jan 31, 2008
65862-198-1010 BLISTER PACK in 1 CARTON (65862-198-10) / 10 CAPSULE in 1 BLISTER PACKJan 31, 2008
65862-198-18180 CAPSULE in 1 BOTTLE (65862-198-18)Apr 29, 2021
65862-198-27270 CAPSULE in 1 BOTTLE (65862-198-27)Apr 29, 2021
65862-198-9090 CAPSULE in 1 BOTTLE (65862-198-90)Apr 29, 2021
65862-198-991000 CAPSULE in 1 BOTTLE (65862-198-99)Jan 31, 2008

Recalls mentioning this NDC

Other Gabapentin products