Hydroxyzine Hydrochloride
- Product NDC
- 63629-1855
- 11-digit product format
- 636291855
- Labeler code
- 63629
- Product ID
- 63629-1855_069fee9d-e252-478e-94a3-f76e7145928a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA087294
- Marketing category
- ANDA
- Marketing start
- 1995-03-09
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE HYDROCHLORIDE
- Active strength
- 10 mg/5mL
- Pharmacologic classes
- Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1855-1 | 63629185501 | 120 mL in 1 BOTTLE (63629-1855-1) | 120 ml | 2004-12-27 | 0000-00-00 | No | No | Current |
| 63629-1855-2 | 63629185502 | 240 mL in 1 BOTTLE (63629-1855-2) | 240 ml | 2004-12-27 | 0000-00-00 | No | No | Current |