Diphenhydramine Hydrochloride Capsule, Liquid Filled
NDC Package 53345-005-01
Package Information
Diphenhydramine Hydrochloride capsules is adults and children 12 years of age and over: 1 softgel (50 mg) at bedtime if needed, or as directed by a doctor. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Humanwell Puracap Pharmaceutical (wuhan), Ltd., this product is identified by NDC 53345-005 and is authorized under FDA application M010.
Identification & Billing
- RxCUI: 1020477 - diphenhydrAMINE HCl 50 MG Oral Capsule
- RxCUI: 1020477 - diphenhydramine hydrochloride 50 MG Oral Capsule
- RxCUI: 1020477 - diphenhydramine HCl 50 MG Oral Capsule
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 53345 - Humanwell Puracap Pharmaceutical (wuhan), Ltd.
- 53345-005 - Diphenhydramine Hydrochloride
- 53345-005-01 - 1 BAG in 1 BOX / 12000 CAPSULE, LIQUID FILLED in 1 BAG
- 53345-005 - Diphenhydramine Hydrochloride
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.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (53345-005). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 53345-005-01 identifies a specific commercial package of 1 bag in 1 box / 12000 capsule, liquid filled in 1 bag of Diphenhydramine Hydrochloride, a human over the counter drug labeled by Humanwell Puracap Pharmaceutical (wuhan), Ltd.. This capsule, liquid filled is formulated for oral use and contains diphenhydramine hydrochloride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Humanwell Puracap Pharmaceutical (wuhan), Ltd. on April 15, 2013. The current certification is valid through December 31, 2026.
How is this Humanwell Puracap Pharmaceutical (wuhan), Ltd. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 53345000501. 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 Product segment to maintain the 5-4-2 structure.