0143-9993 NDC - GABAPENTIN ()

Drug Information

Product NDC: 0143-9993

Proprietary Name: Gabapentin

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: West-ward Pharmaceutical Corp
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/9/2007

Package Information

No. Package Code Package Description Billing Unit
10143-9993-01100 CAPSULE in 1 BOTTLE (0143-9993-01)EA
20143-9993-05500 CAPSULE in 1 BOTTLE (0143-9993-05)
30143-9993-101000 CAPSULE in 1 BOTTLE (0143-9993-10)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0143-9993The 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 DATE7/9/2007This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWest-ward Pharmaceutical CorpName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 10/4/2019