63691-002 NDC - ANTIBACTERIAL ()

Drug Information

Product NDC: 63691-002

Proprietary Name: Antibacterial

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	63691-002-01	304 mL in 1 BOTTLE (63691-002-01)
2	63691-002-02	384 mL in 1 BOTTLE (63691-002-02)
3	63691-002-03	414 mL in 1 BOTTLE (63691-002-03)
4	63691-002-04	739 mL in 1 BOTTLE (63691-002-04)
5	63691-002-05	828 mL in 1 BOTTLE (63691-002-05)
6	63691-002-06	1120 mL in 1 BOTTLE (63691-002-06)
7	63691-002-07	1770 mL in 1 BOTTLE (63691-002-07)
8	63691-002-08	3785 mL in 1 BOTTLE (63691-002-08)
9	63691-002-09	3990 mL in 1 BOTTLE (63691-002-09)
10	63691-002-10	709 mL in 1 BOTTLE (63691-002-10)
11	63691-002-11	1005 mL in 1 BOTTLE (63691-002-11)

Field Name	Field Value	Definition
PRODUCT NDC	63691-002	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	Antibacterial	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	2/13/1998	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Sun Products Corporation	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