hydroxyzine pamoate
- Product NDC
- 63629-8183
- 11-digit product format
- 636298183
- Labeler code
- 63629
- Product ID
- 63629-8183_20d9a2c4-5fa7-46d4-b7f1-9498b3405d62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine pamoate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201507
- Marketing category
- ANDA
- Marketing start
- 2013-06-03
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE PAMOATE
- Active strength
- 25 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| M20215MUFR | HYDROXYZINE PAMOATE | 10246-75-0 | HYDROXYZINE PAMOATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8183-1 | 63629818301 | 30 CAPSULE in 1 BOTTLE (63629-8183-1) | 30 capsule | 2019-07-19 | 0000-00-00 | No | No | Current |