Benadryl Ultratabs 25 mg/1
DIPHENHYDRAMINE HYDROCHLORIDE · TABLET, FILM COATED · Navajo Manufacturing Company Inc.
Benadryl Ultratabs is a tablet, film coated containing diphenhydramine hydrochloride at 25 mg/1, taken oral. Manufactured by Navajo Manufacturing Company Inc..
Key Facts
- Brand Name
- Benadryl Ultratabs
- Generic Name
- DIPHENHYDRAMINE HYDROCHLORIDE
- NDC Code (Product)
67751-166- Manufacturer
- Navajo Manufacturing Company Inc.
- Strength
- 25 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- M012
- Marketing Start
- 09/22/2016
Recall History
No Recall HistoryFrequently Asked Questions
What is Benadryl Ultratabs used for?
Benadryl Ultratabs contains DIPHENHYDRAMINE HYDROCHLORIDE. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is Benadryl Ultratabs a controlled substance?
Benadryl Ultratabs is not classified as a controlled substance by the DEA.
What is the generic name for Benadryl Ultratabs?
The generic name for Benadryl Ultratabs is DIPHENHYDRAMINE HYDROCHLORIDE. There are 12 other brand versions of DIPHENHYDRAMINE HYDROCHLORIDE.
What is the NDC code for Benadryl Ultratabs 25 mg/1?
The NDC (National Drug Code) for Benadryl Ultratabs 25 mg/1 is 67751-166, listed by Navajo Manufacturing Company Inc..
Other Diphenhydramine Brands
See all →- TopCare health NIGHTTIME MAXIMUM STRENGTH Sleep Aid50 mg/176162-438
- Sleep Aid25 mg/176168-015
- Allergy25 mg/176168-121
- NIGHTTIME SLEEP AID25 mg/179903-083
- Allergy Relief25 mg/183059-0021
- Banophen2 g/100g0904-5354
- Diphenhydramine Hydrochloride25 mg/10904-7237
- Nighttime Sleep Aid50 mg/30mL11673-285
- Anti-itch20 mg/g11673-895
- Topcare childrens allergy12.5 mg/5mL36800-379
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)