NDC 69267-201 Propranolol Scopolamine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69267 - Tps
- 69267-201 - Propranolol Scopolamine
Product Characteristics
Product Packages
NDC Code 69267-201-06
Package Description: 121.5 mg in 1 BOTTLE, PLASTIC
NDC Code 69267-201-12
Package Description: 243 mg in 1 BOTTLE, PLASTIC
NDC Code 69267-201-24
Package Description: 486 mg in 1 BOTTLE, PLASTIC
NDC Code 69267-201-48
Package Description: 972 mg in 1 BOTTLE, PLASTIC
Product Details
What is NDC 69267-201?
Which are Propranolol Scopolamine UNII Codes?
The UNII codes for the active ingredients in this product are:
- SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB)
- SCOPOLAMINE (UNII: DL48G20X8X) (Active Moiety)
- PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V)
- PROPRANOLOL (UNII: 9Y8NXQ24VQ) (Active Moiety)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".