NDC 71610-621 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-621

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
October 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (10)

Package NDCDescriptionSince
71610-621-1515 TABLET in 1 BOTTLE (71610-621-15)Jan 24, 2022
71610-621-3030 TABLET in 1 BOTTLE (71610-621-30)Dec 2, 2021
71610-621-4545 TABLET in 1 BOTTLE (71610-621-45)Dec 2, 2021
71610-621-5360 TABLET in 1 BOTTLE (71610-621-53)Jan 24, 2022
71610-621-6090 TABLET in 1 BOTTLE (71610-621-60)Dec 2, 2021
71610-621-70120 TABLET in 1 BOTTLE (71610-621-70)Jan 24, 2022
71610-621-73135 TABLET in 1 BOTTLE (71610-621-73)Dec 2, 2021
71610-621-80180 TABLET in 1 BOTTLE (71610-621-80)Dec 17, 2021
71610-621-92270 TABLET in 1 BOTTLE (71610-621-92)Dec 2, 2021
71610-621-94360 TABLET in 1 BOTTLE (71610-621-94)Jan 24, 2022

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