Hydroxyzine Hydrochloride
- Product NDC
- 63629-6716
- 11-digit product format
- 636296716
- Labeler code
- 63629
- Product ID
- 63629-6716_78d16e10-7bab-41da-8184-fcbffbdc00e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040808
- Marketing category
- ANDA
- Marketing start
- 2007-06-29
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-6716-1 | 63629671601 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-6716-1) | 2015-08-31 | 0000-00-00 | No | No | Current |
| 63629-6716-2 | 63629671602 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-6716-2) | 2015-08-31 | 0000-00-00 | No | No | Current |
| 63629-6716-3 | 63629671603 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-6716-3) | 2015-08-31 | 0000-00-00 | No | No | Current |
| 63629-6716-4 | 63629671604 | 45 TABLET, FILM COATED in 1 BOTTLE (63629-6716-4) | 2015-08-31 | 0000-00-00 | No | No | Current |
| 63629-6716-5 | 63629671605 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-6716-5) | 2015-08-31 | 0000-00-00 | No | No | Current |