Hydroxyzine Hydrochloride
- Product NDC
- 50090-3286
- 11-digit product format
- 500903286
- Labeler code
- 50090
- Product ID
- 50090-3286_4462b073-7462-49fc-8645-bed809146e51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
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 |
|---|
| 50090-3286-0 | Hydroxyzine Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 5 |
| 50090-3286-1 | Hydroxyzine Hydrochloride | 28 in 1 BOTTLE | TABLET, FILM COATED | 28 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3286 | HYDROXYZINE HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 5 | Legacy NDC, 2 package rows | 20190928_8ae73c6f-7134-42f0-a1ad-5dfafedf5c08.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3286-0 | 50090328600 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3286-0) | 2019-01-31 | 0000-00-00 | No | No | Current |
| 50090-3286-1 | 50090328601 | 28 TABLET, FILM COATED in 1 BOTTLE (50090-3286-1) | 2017-11-30 | 0000-00-00 | No | No | Current |