NDC 16714-662 – Gabapentin

Gabapentin 300 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC16714-662

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
NorthStar Rx LLC
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 (3)

Package NDCDescriptionSince
16714-662-01100 CAPSULE in 1 BOTTLE (16714-662-01)Jan 31, 2008
16714-662-02500 CAPSULE in 1 BOTTLE (16714-662-02)Jan 31, 2008
16714-662-031000 CAPSULE in 1 BOTTLE (16714-662-03)Jan 31, 2008

Recalls mentioning this NDC

Other Gabapentin products