Hydroxyzine Hydrochloride
- Product NDC
- 70518-2240
- 11-digit product format
- 705182240
- Labeler code
- 70518
- Product ID
- 70518-2240_8f033b90-d092-6c1e-e053-2995a90aef46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040604
- Marketing category
- ANDA
- Marketing start
- 2019-07-31
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record