Hydroxyzine Hydrochloride
- Product NDC
- 63629-7675
- 11-digit product format
- 636297675
- Labeler code
- 63629
- Product ID
- 63629-7675_f3818354-fd2d-4923-b42e-92f24c27e9be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA088618
- Marketing category
- ANDA
- Marketing start
- 2012-10-09
- 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
- 2020-12-31
- 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 |
|---|
| 63629-7675-1 | 63629767501 | 12 TABLET, FILM COATED in 1 BOTTLE (63629-7675-1) | 2019-04-11 | 0000-00-00 | No | No | Current |
| 63629-7675-2 | 63629767502 | 16 TABLET, FILM COATED in 1 BOTTLE (63629-7675-2) | 2019-04-11 | 0000-00-00 | No | No | Current |
| 63629-7675-3 | 63629767503 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7675-3) | 2019-04-11 | 0000-00-00 | No | No | Current |