49288-0572 NDC - THYME ()

Drug Information

No.	Package Code	Package Description
1	49288-0572-1	2 mL in 1 VIAL, MULTI-DOSE (49288-0572-1)
2	49288-0572-2	5 mL in 1 VIAL, MULTI-DOSE (49288-0572-2)
3	49288-0572-3	10 mL in 1 VIAL, MULTI-DOSE (49288-0572-3)
4	49288-0572-4	30 mL in 1 VIAL, MULTI-DOSE (49288-0572-4)
5	49288-0572-5	50 mL in 1 VIAL, MULTI-DOSE (49288-0572-5)

Field Name	Field Value	Definition
PRODUCT NDC	49288-0572	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	Thyme	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	3/23/1974	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	BLA	The translation of the dosage form Code submitted by the firm.
APPLICATION NUMBER	BLA102223	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	Antigen Laboratories, Inc.	This is the date that the labeler indicates was the start of its marketing of the drug product.