16103-376 NDC - PHARBETOL ()

Drug Information

Product NDC: 16103-376

Proprietary Name: Pharbetol

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Pharbest Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	1/10/2006

No.	Package Code	Package Description	Billing Unit
1	16103-376-06	1 BOTTLE, PLASTIC in 1 CARTON (16103-376-06) / 50 TABLET in 1 BOTTLE, PLASTIC	EA
2	16103-376-08	1 BOTTLE, PLASTIC in 1 CARTON (16103-376-08) / 100 TABLET in 1 BOTTLE, PLASTIC	EA
3	16103-376-11	1000 TABLET in 1 BOTTLE, PLASTIC (16103-376-11)	EA

Field Name	Field Value	Definition
PRODUCT NDC	16103-376	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	Pharbetol	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	1/10/2006	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Pharbest Pharmaceuticals, Inc.	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