Hydroxyzine Hydrochloride
- Product NDC
- 60687-686
- 11-digit product format
- 606870686
- Labeler code
- 60687
- Product ID
- 60687-686_e5c1cd5a-fa60-704b-e053-2995a90a1ab7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA088619
- Marketing category
- ANDA
- Marketing start
- 2022-08-20
- 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-686-01 | Hydroxyzine Hydrochloride | 100 in 1 CARTON | TABLET, FILM COATED | 100 | | 2 |
| 60687-686-11 | Hydroxyzine Hydrochloride | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60687-686 | HYDROXYZINE HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 2 | Legacy NDC, 2 package rows | 20240926_47bda4fe-ddb7-4140-900a-970373cc7acc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-686-01 | 60687068601 | 100 BLISTER PACK in 1 CARTON (60687-686-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-686-11) | 100 blister pack | 2022-08-20 | 0000-00-00 | No | No | Current |
| 60687-686-11 | 60687068611 | 1 in 1 BLISTER PACK | | | | | | Historical |