0372-0004 NDC - SCOT-TUSSIN ORIGINAL SF MULTI-SYMPTOM ()

Drug Information

Product NDC: 0372-0004

Proprietary Name: Scot-Tussin Original SF Multi-Symptom

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: SCOT-TUSSIN Pharmacal Co., Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/1/1956

Package Information

No. Package Code Package Description Billing Unit
10372-0004-04118 mL in 1 BOTTLE (0372-0004-04)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0372-0004The 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 NAMEScot-Tussin Original SF Multi-SymptomThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/1/1956This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESCOT-TUSSIN Pharmacal Co., Inc.Name 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