Hydroxyzine Hydrochloride
- Product NDC
- 55700-760
- 11-digit product format
- 557000760
- Labeler code
- 55700
- Product ID
- 55700-760_624666ad-f09b-4bcf-9c5b-ed036ab6673a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA088619
- Marketing category
- ANDA
- Marketing start
- 2019-05-31
- 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 |
|---|
| 55700-760-30 | 55700076030 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-760-30) | 2019-10-11 | 0000-00-00 | No | No | Current |
| 55700-760-60 | 55700076060 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-760-60) | 2019-10-11 | 0000-00-00 | No | No | Current |
| 55700-760-90 | 55700076090 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-760-90) | 2019-05-31 | 0000-00-00 | No | No | Current |