Hydroxyzine Hydrochloride
- Product NDC
- 60429-225
- 11-digit product format
- 604290225
- Labeler code
- 60429
- Product ID
- 60429-225_c0963042-9c21-e2a6-e053-2995a90a5720
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA040808
- Marketing category
- ANDA
- Marketing start
- 2008-09-24
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-225-01 | 60429022501 | 100 TABLET, FILM COATED in 1 BOTTLE (60429-225-01) | 2008-09-24 | 0000-00-00 | No | No | Current |
| 60429-225-05 | 60429022505 | 500 TABLET, FILM COATED in 1 BOTTLE (60429-225-05) | 2008-09-24 | 0000-00-00 | No | No | Current |