hydroxyzine pamoate
- Product NDC
- 58118-0025
- 11-digit product format
- 581180025
- Labeler code
- 58118
- Product ID
- 58118-0025_f1ea65fe-0b6f-c643-e053-2995a90aefaa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine pamoate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Clinical Solutions Wholsesale
- 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
- 2024-12-31
- 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 |
|---|
| 58118-0025-8 | 58118002508 | 30 CAPSULE in 1 BLISTER PACK (58118-0025-8) | 30 capsule | 2015-09-15 | 0000-00-00 | No | No | Current |