Hydroxyzine Hydrochloride
- Product NDC
- 50090-0276
- 11-digit product format
- 500900276
- Labeler code
- 50090
- Product ID
- 50090-0276_3d855943-98cc-4ce8-bd9b-841a99cb6eef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0276-1 | 50090027601 | 118 mL in 1 BOTTLE, PLASTIC (50090-0276-1) | 118 ml | 2016-06-29 | 0000-00-00 | No | No | Current |