Hydroxyzine Hydrochloride
- Product NDC
- 0378-2587
- 11-digit product format
- 003782587
- Labeler code
- 0378
- Product ID
- 0378-2587_00b7c512-5d41-4218-870f-9838716c761e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA091176
- Marketing category
- ANDA
- Marketing start
- 2010-07-23
- Marketing end
- 2019-07-31
- Substance
- HYDROXYZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record