Hydroxyzine Hydrochloride
- Product NDC
- 60760-971
- 11-digit product format
- 607600971
- Labeler code
- 60760
- Product ID
- 60760-971_1767b4b1-074c-3373-e063-6294a90aca05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA088618
- Marketing category
- ANDA
- Marketing start
- 2012-10-09
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-971-30 | 60760097130 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-971-30) | 2024-04-09 | No | No | Historical |