Hydroxyzine Hydrochloride
- Product NDC
- 68788-9737
- 11-digit product format
- 687889737
- Labeler code
- 68788
- Product ID
- 68788-9737_0fef0d55-2496-44e2-bd4e-f792dc273889
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA040786
- Marketing category
- ANDA
- Marketing start
- 2012-10-08
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE HYDROCHLORIDE
- Active strength
- 10 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