NDC 67877-429 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67877-429

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206402
Marketed since
November 1, 2015
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
67877-429-01100 TABLET in 1 BOTTLE (67877-429-01)Nov 1, 2015
67877-429-05500 TABLET in 1 BOTTLE (67877-429-05)Nov 1, 2015
67877-429-101000 TABLET in 1 BOTTLE (67877-429-10)Nov 1, 2015
67877-429-38100 BLISTER PACK in 1 CARTON (67877-429-38) / 10 TABLET in 1 BLISTER PACKNov 1, 2015

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