Hydroxyzine Hydrochloride
- Product NDC
- 71335-1068
- 11-digit product format
- 713351068
- Labeler code
- 71335
- Product ID
- 71335-1068_4fea2f8d-b95d-4c6a-aa58-c6322e1af97f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040786
- Marketing category
- ANDA
- Marketing start
- 2012-07-24
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71335-1068-1 | 71335106801 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1068-1) | 2019-01-25 | 0000-00-00 | No | No | Current |
| 71335-1068-2 | 71335106802 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1068-2) | 2019-01-25 | 0000-00-00 | No | No | Current |
| 71335-1068-3 | 71335106803 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1068-3) | 2019-01-25 | 0000-00-00 | No | No | Current |
| 71335-1068-4 | 71335106804 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1068-4) | 2019-01-25 | 0000-00-00 | No | No | Current |
| 71335-1068-5 | 71335106805 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1068-5) | 2019-01-25 | 0000-00-00 | No | No | Current |