Nighttime
NDC Package 51672-2113-7
Package Information
Nighttime is a . Marketed by Taro Pharmaceuticals U.s.a. Inc., this product is identified by NDC 51672-2113 and is authorized under FDA application part341.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 51672 - Taro Pharmaceuticals U.s.a. Inc.
- 51672-2113 - Nighttime
- 51672-2113-7 - 6 POWDER, FOR SOLUTION in 1 CARTON
- 51672-2113 - Nighttime
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 51672-2113-7 identifies a specific commercial package of 6 powder, for solution in 1 carton of Nighttime Flu And Severe, labeled by Taro Pharmaceuticals U.s.a. 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 Taro Pharmaceuticals U.s.a. Inc. on June 28, 2013. The current certification is valid through January 17, 2020.
How is this Taro Pharmaceuticals U.s.a. Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 51672211307. 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 Package segment to maintain the 5-4-2 structure.