75847-1713 NDC - DR. IASO AC BOOSTER ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	75847-1713-1	30 mL in 1 BOTTLE, DROPPER (75847-1713-1)

Field Name	Field Value	Definition
PRODUCT NDC	75847-1713	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	DR. IASO AC BOOSTER	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
START MARKETING DATE	8/1/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	12/31/2023	This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAME	UNAPPROVED DRUG OTHER	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	IASO Inc	Name of Company corresponding to the labeler code segment of the Product NDC.