Hydroxyzine hydrochloride
- Product NDC
- 70518-2807
- 11-digit product format
- 705182807
- Labeler code
- 70518
- Product ID
- 70518-2807_4aa35fdf-9b24-64c4-e063-6294a90a7e60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204279
- Marketing category
- ANDA
- Marketing start
- 2020-07-08
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hydroxyzine hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROXYZINE DIHYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 76755771U3 |
| Rxcui | 995218 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2807-0 | Hydroxyzine hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2807 | HYDROXYZINE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250403_71eea118-395c-4559-aed5-900b635674b8.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 |
|---|
| 70518-2807-0 | 70518280700 | 30 TABLET in 1 BLISTER PACK (70518-2807-0) | 30 tablet | 2020-07-08 | 0000-00-00 | No | No | Current |