hydroxyzine pamoate
- Product NDC
- 55700-742
- 11-digit product format
- 557000742
- Labeler code
- 55700
- Product ID
- 55700-742_cbb4a17b-f45c-401b-8d71-0da4a16bff8a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine pamoate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA086183
- Marketing category
- ANDA
- Marketing start
- 2019-04-11
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE PAMOATE
- Active strength
- 50 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 |
|---|
| 55700-742-90 | 55700074290 | 90 CAPSULE in 1 BOTTLE (55700-742-90) | 90 capsule | 2019-04-11 | 0000-00-00 | No | No | Current |