Hydroxyzine Hydrochloride
- Product NDC
- 66267-112
- 11-digit product format
- 662670112
- Labeler code
- 66267
- Product ID
- 66267-112_b8a719a1-e1f2-64d7-e053-2a95a90a4f25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA040804
- Marketing category
- ANDA
- Marketing start
- 2008-06-30
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE HYDROCHLORIDE
- Active strength
- 10 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66267-112-15 | 66267011215 | 15 TABLET, FILM COATED in 1 BOTTLE (66267-112-15) | 2016-10-06 | 0000-00-00 | No | No | Current |
| 66267-112-30 | 66267011230 | 30 TABLET, FILM COATED in 1 BOTTLE (66267-112-30) | 2016-10-06 | 0000-00-00 | No | No | Current |