NDC 85509-1166 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC85509-1166

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
PHOENIX RX LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
October 1, 2021
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (3)

Package NDCDescriptionSince
85509-1166-330 TABLET in 1 BOTTLE (85509-1166-3)Sep 2, 2026
85509-1166-660 TABLET in 1 BOTTLE (85509-1166-6)Sep 2, 2026
85509-1166-990 TABLET in 1 BOTTLE (85509-1166-9)Sep 2, 2026

Other Gabapentin products