53149-4852 NDC - CYCLOBENZAPRINE HYDROCHLORIDE ()

Drug Information

Product NDC: 53149-4852

Proprietary Name: Cyclobenzaprine Hydrochloride

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	53149-4852-1	120 TABLET, FILM COATED in 1 BOTTLE (53149-4852-1)	EA
2	53149-4852-3	30 TABLET, FILM COATED in 1 BOTTLE (53149-4852-3)	EA
3	53149-4852-6	60 TABLET, FILM COATED in 1 BOTTLE (53149-4852-6)	EA
4	53149-4852-9	90 TABLET, FILM COATED in 1 BOTTLE (53149-4852-9)	EA

Field Name	Field Value	Definition
PRODUCT NDC	53149-4852	The 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 NAME	Cyclobenzaprine Hydrochloride	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	8/1/2017	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	All Pharma, LLC	Name of Company corresponding to the labeler code segment of the Product NDC.

Export to text format icon Download this NDC record in Text format: Export

Export to text format icon Download this NDC record in Excel (CSV) format: Export

Export to text format icon Download this NDC record in XML format: Export

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