Diphenhydramine Hydrochloride
- Product NDC
- 50090-7014
- 11-digit product format
- 500907014
- Labeler code
- 50090
- Product ID
- 50090-7014_59ecc4f3-dc0e-4d7e-a47c-f00601d9228c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-04-14
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| TC2D6JAD40 | DIPHENHYDRAMINE HYDROCHLORIDE | 147-24-0 | DIPHENHYDRAMINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7014-0 | 50090701400 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-7014-0) / 10 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2024-01-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| 0835K- Major | A-S Medication Solutions | 2024-03-12 | HUMAN OTC DRUG LABEL | 3 |