Drugplain

Benadryl Ultra Tab 25 mg/1

DIPHENHYDRAMINE HYDROCHLORIDE · TABLET, FILM COATED · JC World Bell Wholesale Co., Inc.

No Recall History
Plain English

Benadryl Ultra Tab is a tablet, film coated containing diphenhydramine hydrochloride at 25 mg/1, taken oral. Manufactured by JC World Bell Wholesale Co., Inc..

Key Facts

Brand Name
Benadryl Ultra Tab
Generic Name
DIPHENHYDRAMINE HYDROCHLORIDE
NDC Code (Product)
50269-226
Manufacturer
JC World Bell Wholesale Co., Inc.
Strength
25 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
08/16/2018

Recall History

No Recall History

Frequently Asked Questions

What is Benadryl Ultra Tab used for?

Benadryl Ultra Tab contains DIPHENHYDRAMINE HYDROCHLORIDE. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Benadryl Ultra Tab a controlled substance?

Benadryl Ultra Tab is not classified as a controlled substance by the DEA.

What is the generic name for Benadryl Ultra Tab?

The generic name for Benadryl Ultra Tab is DIPHENHYDRAMINE HYDROCHLORIDE. There are 12 other brand versions of DIPHENHYDRAMINE HYDROCHLORIDE.

What is the NDC code for Benadryl Ultra Tab 25 mg/1?

The NDC (National Drug Code) for Benadryl Ultra Tab 25 mg/1 is 50269-226, listed by JC World Bell Wholesale Co., Inc..