Hydroxyzine Hydrochloride
- Product NDC
- 55154-5377
- 11-digit product format
- 551545377
- Labeler code
- 55154
- Product ID
- 55154-5377_3ce73974-6fb5-48bc-b04d-e9f18d6e062c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA091176
- Marketing category
- ANDA
- Marketing start
- 2010-07-23
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record