Benadryl Ultra Tab
- Product NDC
- 50269-226
- Requested package NDC
- 50269-226-54
- 11-digit product format
- 502690226
- Labeler code
- 50269
- Product ID
- 50269-226_dc798c4b-f16f-5a80-e053-2995a90a0a06
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIPHENHYDRAMINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- JC World Bell Wholesale Co., Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-08-16
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50269-226-54 | Benadryl Ultra Tab | 25 in 1 BOX | TABLET, FILM COATED | 25 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50269-226 | BENADRYL ULTRA TAB (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [JC WORLD BELL WHOLESALE CO., INC.] | 4 | Legacy NDC, 1 package rows | 20250101_17633c87-ff0f-4fde-ab23-bc43bdc3fa8e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50269-226-54 | 50269022654 | 25 TABLET, FILM COATED in 1 BOX (50269-226-54) | 2018-08-16 | 0000-00-00 | No | No | Current |