Hydroxyzine HCL
- Product NDC
- 72189-577
- 11-digit product format
- 721890577
- Labeler code
- 72189
- Product ID
- 72189-577_22049012-733f-6b45-e063-6294a90a670f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine HCL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_rx
- Application
- ANDA217652
- Marketing category
- ANDA
- Marketing start
- 2024-09-13
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-577-60 | 72189057760 | 60 TABLET, FILM COATED in 1 BOTTLE (72189-577-60) | 2024-09-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Hydroxyzine HCL | Direct_rx | 2024-09-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |