HydrOXYzine Hydrochloride
- Product NDC
- 50090-6626
- 11-digit product format
- 500906626
- Labeler code
- 50090
- Product ID
- 50090-6626_3aa1348c-dc6e-4500-abdc-9170862a52c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HydrOXYzine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040840
- Marketing category
- ANDA
- Marketing start
- 2009-11-11
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 76755771U3 | HYDROXYZINE HYDROCHLORIDE | 2192-20-3 | HydrOXYzine Hydrochloride |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6626-0 | 50090662600 | 90 TABLET in 1 BOTTLE (50090-6626-0) | 90 tablet | 2023-08-25 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rx Only | A-S Medication Solutions | 2023-09-07 | Human Prescription Drug Label | 3 |