43353-709 NDC - GABAPENTIN ()

Drug Information

Product NDC: 43353-709

Proprietary Name: Gabapentin

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Aphena Pharma Solutions - Tennessee, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/17/2010

Package Information

No. Package Code Package Description Billing Unit
143353-709-3030 CAPSULE in 1 BOTTLE, PLASTIC (43353-709-30)EA
243353-709-5360 CAPSULE in 1 BOTTLE, PLASTIC (43353-709-53)EA
343353-709-6090 CAPSULE in 1 BOTTLE, PLASTIC (43353-709-60)EA
443353-709-70120 CAPSULE in 1 BOTTLE, PLASTIC (43353-709-70)EA
543353-709-80180 CAPSULE in 1 BOTTLE, PLASTIC (43353-709-80)EA
643353-709-92270 CAPSULE in 1 BOTTLE, PLASTIC (43353-709-92)EA
743353-709-94360 CAPSULE in 1 BOTTLE, PLASTIC (43353-709-94)EA
843353-709-98540 CAPSULE in 1 BOTTLE, PLASTIC (43353-709-98)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC43353-709The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEGabapentinThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/17/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAphena Pharma Solutions - Tennessee, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023