hydroxyzine pamoate
- Product NDC
- 70518-1659
- 11-digit product format
- 705181659
- Labeler code
- 70518
- Product ID
- 70518-1659_87750d5d-e817-e635-e053-2a95a90adcf3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine pamoate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA086183
- Marketing category
- ANDA
- Marketing start
- 2018-11-12
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE PAMOATE
- 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