71335-1453 NDC - GABAPENTIN ()

Drug Information

Product NDC: 71335-1453

Proprietary Name: GABAPENTIN

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Bryant Ranch Prepack
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/5/2017

Package Information

No. Package Code Package Description Billing Unit
171335-1453-020 CAPSULE in 1 BOTTLE (71335-1453-0)
271335-1453-130 CAPSULE in 1 BOTTLE (71335-1453-1)
371335-1453-290 CAPSULE in 1 BOTTLE (71335-1453-2)EA
471335-1453-360 CAPSULE in 1 BOTTLE (71335-1453-3)
571335-1453-4120 CAPSULE in 1 BOTTLE (71335-1453-4)
671335-1453-5100 CAPSULE in 1 BOTTLE (71335-1453-5)
771335-1453-628 CAPSULE in 1 BOTTLE (71335-1453-6)
871335-1453-7112 CAPSULE in 1 BOTTLE (71335-1453-7)
971335-1453-884 CAPSULE in 1 BOTTLE (71335-1453-8)
1071335-1453-9180 CAPSULE in 1 BOTTLE (71335-1453-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71335-1453The 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 DATE12/5/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBryant Ranch PrepackName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024