Hydroxyzine Hydrochloride
- Product NDC
- 68071-5086
- 11-digit product format
- 680715086
- Labeler code
- 68071
- Product ID
- 68071-5086_bbb7a70c-5100-13be-e053-2a95a90acaf6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040786
- Marketing category
- ANDA
- Marketing start
- 2012-07-24
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5086-3 | 68071508603 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-5086-3) | 2019-10-17 | 0000-00-00 | No | No | Current |