Hydroxyzine
- Product NDC
- 52584-601
- 11-digit product format
- 525840601
- Labeler code
- 52584
- Product ID
- 52584-601_e711ee73-c054-4f3f-a189-bb3c01c7aecc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA087408
- Marketing category
- ANDA
- Marketing start
- 2010-03-01
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Active strength
- 50 mg/mL
- 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 |
|---|
| 52584-601-25 | 52584060125 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-601-25) > 1 mL in 1 VIAL, SINGLE-DOSE | 2010-03-01 | 0000-00-00 | No | No | Current |