NDC 71610-737 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-737

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
February 4, 2016
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (8)

Package NDCDescriptionSince
71610-737-3030 TABLET in 1 BOTTLE (71610-737-30)Sep 22, 2023
71610-737-4545 TABLET in 1 BOTTLE (71610-737-45)Sep 22, 2023
71610-737-5360 TABLET in 1 BOTTLE (71610-737-53)Sep 22, 2023
71610-737-6090 TABLET in 1 BOTTLE (71610-737-60)Sep 22, 2023
71610-737-70120 TABLET in 1 BOTTLE (71610-737-70)Sep 22, 2023
71610-737-73135 TABLET in 1 BOTTLE (71610-737-73)Sep 22, 2023
71610-737-80180 TABLET in 1 BOTTLE (71610-737-80)Sep 22, 2023
71610-737-92270 TABLET in 1 BOTTLE (71610-737-92)Sep 22, 2023

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