NDC Code 49288-9933-1
Package Description: 2 mL in 1 VIAL
NDC Code 49288-9933-2
Package Description: 4 mL in 1 VIAL
NDC Code 49288-9933-3
Package Description: 4.5 mL in 1 VIAL
NDC Code 49288-9933-4
Package Description: 8 mL in 1 VIAL
NDC Code 49288-9933-5
Package Description: 9 mL in 1 VIAL
NDC Code 49288-9933-6
Package Description: 24 mL in 1 VIAL
NDC Code 49288-9933-7
Package Description: 30 mL in 1 VIAL
NDC Code 49288-9933-8
Package Description: 100 mL in 1 VIAL
NDC Code 49288-9933-9
Package Description: 40 mL in 1 VIAL
 What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
 What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
 What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
 What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".