55714-2322 NDC - MORNING SICKNESS ()

Drug Information

No.	Package Code	Package Description
1	55714-2322-0	.5 mL in 1 BOTTLE, GLASS (55714-2322-0)
2	55714-2322-1	29.57 mL in 1 BOTTLE, GLASS (55714-2322-1)
3	55714-2322-2	59.14 mL in 1 BOTTLE, GLASS (55714-2322-2)

Field Name	Field Value	Definition
PRODUCT NDC	55714-2322	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	Morning Sickness	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	3/1/2011	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Newton Laboratories, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.