66521-200 NDC - INFLUENZA A (H1N1) 2009 MONOVALENT VACCINE ()

Drug Information

Product NDC: 66521-200

Proprietary Name: Influenza A (H1N1) 2009 Monovalent Vaccine

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Novartis Vaccines and Diagnostics Ltd
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	9/15/2009

No.	Package Code	Package Description	Billing Unit
1	66521-200-02	10 SYRINGE, GLASS in 1 CARTON (66521-200-02) / .5 mL in 1 SYRINGE, GLASS	ML
2	66521-200-10	1 VIAL, MULTI-DOSE in 1 CARTON (66521-200-10) / 5 mL in 1 VIAL, MULTI-DOSE

Field Name	Field Value	Definition
PRODUCT NDC	66521-200	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	Influenza A (H1N1) 2009 Monovalent Vaccine	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	9/15/2009	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Novartis Vaccines and Diagnostics Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023