10481-1053 NDC - SILVER NITRATE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	10481-1053-1	30 g in 1 BOTTLE, GLASS (10481-1053-1)	ML

Field Name	Field Value	Definition
PRODUCT NDC	10481-1053	This is the date that the labeler indicates was the start of its marketing of the drug product.
PROPRIETARY NAME	Silver Nitrate	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	7/14/2010	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	11/1/2021	Name of Company corresponding to the labeler code segment of the Product NDC.
MARKETING CATEGORY NAME	UNAPPROVED DRUG OTHER	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Gordon Laboratories	Name of Company corresponding to the labeler code segment of the Product NDC.