NDC 69267-202 Propranolol Scopolamine

  1. Labeler Index
  2. Tps
  3. NDC: 69267-202 Propranolol Scopolamine

NDC Product Code 69267-202

NDC CODE: 69267-202

Proprietary Name: Propranolol Scopolamine What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

Color(s):
WHITE (C48325)
Shape: ROUND (C48348)
Size(s):
5 MM
Score: 1

NDC Code Structure

NDC 69267-202-06

Package Description: 243 mg in 1 BOTTLE, PLASTIC

NDC 69267-202-12

Package Description: 486 mg in 1 BOTTLE, PLASTIC

NDC 69267-202-24

Package Description: 972 mg in 1 BOTTLE, PLASTIC

NDC 69267-202-48

Package Description: 1944 mg in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Propranolol Scopolamine with NDC 69267-202 is a product labeled by Tps. The generic name of Propranolol Scopolamine is . The product's dosage form is and is administered via form.

Labeler Name: Tps

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Tps
Labeler Code: 69267
Start Marketing Date: 10-01-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 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.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Propranolol Scopolamine Product Label Images

Propranolol Scopolamine Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Instructions For Use

Take one tablet orally as directed by your physician as needed for symptoms of panic or anxiety.Do not exceed two tablets per day.

* Please review the disclaimer below.