Hydroxyzine pamoate
- Product NDC
- 70518-3323
- 11-digit product format
- 705183323
- Labeler code
- 70518
- Product ID
- 70518-3323_d4dd5a09-a013-2346-e053-2a95a90aa6d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine pamoate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA011459
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-12-29
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3323-0 | 70518332300 | 30 CAPSULE in 1 BLISTER PACK (70518-3323-0) | 30 capsule | 2021-12-29 | 0000-00-00 | No | No | Current |