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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 Information

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

Package Information

No. Package Code Package Description Billing Unit
166521-200-0210 SYRINGE, GLASS in 1 CARTON (66521-200-02) / .5 mL in 1 SYRINGE, GLASSML
266521-200-101 VIAL, MULTI-DOSE in 1 CARTON (66521-200-10) / 5 mL in 1 VIAL, MULTI-DOSE

NDC Record

Field Name Field Value Definition
PRODUCT NDC66521-200The 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 NAMEInfluenza A (H1N1) 2009 Monovalent VaccineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/15/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENovartis Vaccines and Diagnostics LtdName 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