35781-0301 NDC - LIDODOSE ()

Drug Information

Product NDC: 35781-0301

Proprietary Name: Lidodose

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Gensco Laboratories, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2018

Package Information

No. Package Code Package Description Billing Unit
135781-0301-1100 POUCH in 1 BOX (35781-0301-1) / 1 mL in 1 POUCH (35781-0301-0)ML
235781-0301-525 POUCH in 1 BOX (35781-0301-5) / 1 mL in 1 POUCH (35781-0301-0)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC35781-0301The 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 NAMELidodoseThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGensco Laboratories, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024