Diphenhydramine HCL
- Product NDC
- 72789-532
- 11-digit product format
- 727890532
- Labeler code
- 72789
- Product ID
- 72789-532_43800734-7ff6-fb15-e063-6394a90aa530
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine HCL
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2010-01-27
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Diphenhydramine HCL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TC2D6JAD40 |
| Rxcui | 1020477 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-532-20 | Diphenhydramine HCL | 20 in 1 BOTTLE, PLASTIC | CAPSULE | 20 | | 5 |
| 72789-532-30 | Diphenhydramine HCL | 30 in 1 BOTTLE, PLASTIC | CAPSULE | 30 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-532-20 | 72789053220 | 20 CAPSULE in 1 BOTTLE, PLASTIC (72789-532-20) | 20 capsule | 2025-11-13 | No | No | Current |
| 72789-532-30 | 72789053230 | 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-532-30) | 30 capsule | 2025-10-16 | No | No | Current |