41391-120 NDC - MYO-BREATHE ()

Drug Information

Product NDC: 41391-120

Proprietary Name: Myo-Breathe

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Myo-Breathe,LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/15/2015

Package Information

No. Package Code Package Description Billing Unit
141391-120-16118 mL in 1 BOTTLE, SPRAY (41391-120-16)
241391-120-19473 mL in 1 BOTTLE, SPRAY (41391-120-19)

NDC Record

Field Name Field Value Definition
PRODUCT NDC41391-120The 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 NAMEMyo-BreatheThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/15/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMyo-Breathe,LLCName 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