hydroxyzine pamoate
- Product NDC
- 55700-237
- 11-digit product format
- 557000237
- Labeler code
- 55700
- Product ID
- 55700-237_5cf1fcab-4ae0-469f-81f8-0db301446376
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine pamoate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA087479
- Marketing category
- ANDA
- Marketing start
- 2014-06-27
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-237-30 | 55700023730 | 30 CAPSULE in 1 BOTTLE (55700-237-30) | 30 capsule | 2015-04-10 | 0000-00-00 | No | No | Current |