HYDROXYZINE PAMOATE
- Product NDC
- 53808-0886
- 11-digit product format
- 538080886
- Labeler code
- 53808
- Product ID
- 53808-0886_1411c929-e5e8-49cd-a165-947ba82b80f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROXYZINE PAMOATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA201507
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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
- 2019-12-31
- 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 |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rx only | State of Florida DOH Central Pharmacy | 2014-10-18 | HUMAN PRESCRIPTION DRUG LABEL | 3 |