79632-222 NDC - SEPTINOL ()

Drug Information

Product NDC: 79632-222

Proprietary Name: Septinol

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Fabulous Innovations LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/10/2020

Package Information

No. Package Code Package Description Billing Unit
179632-222-0150 mL in 1 BOTTLE (79632-222-01)
279632-222-02100 mL in 1 BOTTLE (79632-222-02)
379632-222-03500 mL in 1 BOTTLE (79632-222-03)
479632-222-042000 mL in 1 BOTTLE (79632-222-04)
579632-222-054000 mL in 1 BOTTLE (79632-222-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC79632-222The 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 NAMESeptinolThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/10/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEFabulous Innovations 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