71610-379 NDC - CYCLOBENZAPRINE HYDROCHLORIDE ()

Drug Information

Product NDC: 71610-379

Proprietary Name: Cyclobenzaprine Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Aphena Pharma Solutions - Tennessee, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/4/2006

Package Information

No. Package Code Package Description Billing Unit
171610-379-3030 TABLET, FILM COATED in 1 BOTTLE (71610-379-30)EA
271610-379-4545 TABLET, FILM COATED in 1 BOTTLE (71610-379-45)EA
371610-379-5360 TABLET, FILM COATED in 1 BOTTLE (71610-379-53)EA
471610-379-6090 TABLET, FILM COATED in 1 BOTTLE (71610-379-60)EA
571610-379-80180 TABLET, FILM COATED in 1 BOTTLE (71610-379-80)EA
671610-379-92270 TABLET, FILM COATED in 1 BOTTLE (71610-379-92)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC71610-379The 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 NAMECyclobenzaprine HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/4/2006This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAphena Pharma Solutions - Tennessee, LLCName 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