Antihistamine
- Product NDC
- 77333-231
- 11-digit product format
- 773330231
- Labeler code
- 77333
- Product ID
- 77333-231_50fab60d-a209-cf04-e063-6294a90ab007
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine HCl
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Gendose Pharmaceuticals, LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-15
- 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
- 2027-12-31
- 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 |
|---|
| 77333-231-10 | 77333023110 | 100 BLISTER PACK in 1 BOX (77333-231-10) / 1 CAPSULE in 1 BLISTER PACK (77333-231-25) | 100 blister pack | 2026-05-15 | No | No | Historical |