NDC 76420-836 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76420-836

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Asclemed USA, Inc.
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 (6)

Package NDCDescriptionSince
76420-836-01100 TABLET in 1 BOTTLE (76420-836-01)Aug 7, 2024
76420-836-05500 TABLET in 1 BOTTLE (76420-836-05)Aug 7, 2024
76420-836-12120 TABLET in 1 BOTTLE (76420-836-12)May 21, 2025
76420-836-3030 TABLET in 1 BOTTLE (76420-836-30)Aug 7, 2024
76420-836-6060 TABLET in 1 BOTTLE (76420-836-60)Aug 7, 2024
76420-836-9090 TABLET in 1 BOTTLE (76420-836-90)Aug 7, 2024

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