69267-202 NDC - PROPRANOLOL SCOPOLAMINE ()

Drug Information

Product NDC: 69267-202

Proprietary Name: Propranolol Scopolamine

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	69267-202-06	243 mg in 1 BOTTLE, PLASTIC (69267-202-06)
2	69267-202-12	486 mg in 1 BOTTLE, PLASTIC (69267-202-12)
3	69267-202-24	972 mg in 1 BOTTLE, PLASTIC (69267-202-24)
4	69267-202-48	1944 mg in 1 BOTTLE, PLASTIC (69267-202-48)

Field Name	Field Value	Definition
PRODUCT NDC	69267-202	The 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 NAME	Propranolol Scopolamine	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	10/1/2014	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	TPS	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