41391-119 NDC - MYO-BREATHE ()

Drug Information

Product NDC: 41391-119

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:1/10/2009

Package Information

No. Package Code Package Description Billing Unit
141391-119-115 mL in 1 PACKET (41391-119-11)
241391-119-12118 mL in 1 TUBE (41391-119-12)
341391-119-1389 mL in 1 BOTTLE, WITH APPLICATOR (41391-119-13)
441391-119-19473 mL in 1 BOTTLE, PUMP (41391-119-19)

NDC Record

Field Name Field Value Definition
PRODUCT NDC41391-119The 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 DATE1/10/2009This 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