Hydroxyzine Hydrochloride
- Product NDC
- 63629-7087
- 11-digit product format
- 636297087
- Labeler code
- 63629
- Product ID
- 63629-7087_b4993960-b9e4-44e0-b3a8-4b7d188e949d
- 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 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7087-1 | 63629708701 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7087-1) | 2016-09-16 | 0000-00-00 | No | No | Current |
| 63629-7087-2 | 63629708702 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-7087-2) | 2016-09-16 | 0000-00-00 | No | No | Current |