Meclizine Hydrochloride
- Product NDC
- 50090-5496
- 11-digit product format
- 500905496
- Labeler code
- 50090
- Product ID
- 50090-5496_fb049e17-4f9b-4cfb-b564-b43e050a30bd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-10-30
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC], Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Meclizine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MECLIZINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | HDP7W44CIO |
| Rxcui | 995632 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5496-0 | Meclizine Hydrochloride | 30 in 1 BOTTLE | TABLET, CHEWABLE | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5496 | MECLIZINE HYDROCHLORIDE TABLET, CHEWABLE [A-S MEDICATION SOLUTIONS] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250112_2518b0b6-35ab-49f4-936c-1eafea04b466.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 |
|---|
| 50090-5496-0 | 50090549600 | 30 TABLET, CHEWABLE in 1 BOTTLE (50090-5496-0) | 2021-03-19 | 0000-00-00 | No | No | Current |