Hydroxyzine Hydrochloride
- Product NDC
- 71335-0986
- 11-digit product format
- 713350986
- Labeler code
- 71335
- Product ID
- 71335-0986_677b7c57-05bc-4c04-bf13-bd9b52a2e1fd
- 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
- 50 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0986-1 | 71335098601 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0986-1) | 2018-10-31 | 0000-00-00 | No | No | Current |
| 71335-0986-2 | 71335098602 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0986-2) | 2018-10-31 | 0000-00-00 | No | No | Current |
| 71335-0986-3 | 71335098603 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0986-3) | 2018-10-31 | 0000-00-00 | No | No | Current |
| 71335-0986-4 | 71335098604 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0986-4) | 2018-10-31 | 0000-00-00 | No | No | Current |
| 71335-0986-5 | 71335098605 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0986-5) | 2018-10-31 | 0000-00-00 | No | No | Current |