hydroxyzine pamoate
- Product NDC
- 63629-6642
- 11-digit product format
- 636296642
- Labeler code
- 63629
- Product ID
- 63629-6642_c4f7de56-a6b8-46ff-919f-70fb51145f73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine pamoate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA087479
- Marketing category
- ANDA
- Marketing start
- 1981-12-14
- 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
- 2021-12-31
- 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 |
|---|
| 63629-6642-1 | 63629664201 | 30 CAPSULE in 1 BOTTLE (63629-6642-1) | 30 capsule | 2015-08-10 | 0000-00-00 | No | No | Current |
| 63629-6642-2 | 63629664202 | 120 CAPSULE in 1 BOTTLE (63629-6642-2) | 120 capsule | 2015-08-10 | 0000-00-00 | No | No | Current |