Belladonna Alkaloids With Phenobartbital
NDC Package 0440-7183-20
Package Information
Belladonna Alkaloids With Phenobartbital is based on a review of this drug by the National Academy of Sciences-National Research Council and/or other information, FDA has classified the following indications as “possibly” effective:For use as adjunctive therapy in the treatment of irritable bowel syndrome (irritable colon, spastic colon, mucous colitis) and acute enterocolitis.May also be useful as adjunctive therapy in the treatment of duodenal ulcer. Marketed by Liberty Pharmaceuticals, Inc., this product is identified by NDC 0440-7183.
Identification & Billing
- RxCUI: 1046815 - atropine sulfate 0.0194 MG / hyoscyamine sulfate 0.1037 MG / PHENobarbital 16.2 MG / scopolamine HBr 0.0065 MG Oral Tablet
- RxCUI: 1046815 - atropine sulfate 0.0194 MG / hyoscyamine sulfate 0.1037 MG / phenobarbital 16.2 MG / scopolamine hydrobromide 0.0065 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0440 - Liberty Pharmaceuticals, Inc.
- 0440-7183 - Belladonna Alkaloids With Phenobartbital
- 0440-7183-20 - 20 TABLET in 1 BOTTLE
- 0440-7183 - Belladonna Alkaloids With Phenobartbital
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0440-7183-20 identifies a specific commercial package of 20 tablet in 1 bottle of Belladonna Alkaloids With Phenobartbital, labeled by Liberty Pharmaceuticals, Inc.. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Liberty Pharmaceuticals, Inc. on December 01, 2000. The current certification is valid through December 31, 2018.
How is this Liberty Pharmaceuticals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00440718320. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.