Hydroxyzine hydrochloride
- Product NDC
- 60760-307
- 11-digit product format
- 607600307
- Labeler code
- 60760
- Product ID
- 60760-307_889014c6-6f25-6c10-e053-2995a90a18b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary
- Application
- ANDA204279
- Marketing category
- ANDA
- Marketing start
- 2011-10-31
- Marketing end
- 0000-00-00
- Substance
- HYDROXYZINE HYDROCHLORIDE
- Active strength
- 10 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-307-20 | 60760030720 | 20 TABLET in 1 BOTTLE, PLASTIC (60760-307-20) | 20 tablet | 2011-10-31 | 0000-00-00 | No | No | Current |