Hydroxyzine Hydrochloride
- Product NDC
- 68084-255
- 11-digit product format
- 680840255
- Labeler code
- 68084
- Product ID
- 68084-255_de592900-2fd6-7409-e053-2995a90abb13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA040786
- Marketing category
- ANDA
- Marketing start
- 2009-01-14
- Marketing end
- 2022-12-31
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-255-01 | 68084025501 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-255-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-255-11) | 100 blister pack | 2009-01-14 | 0000-00-00 | No | No | Current |