Meclizine Hydrochloride
- Product NDC
- 24689-146
- 11-digit product format
- 246890146
- Labeler code
- 24689
- Product ID
- 24689-146_2b4a3632-89d2-8d7d-e063-6294a90a71e1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- APNAR PHARMA LP
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-11-21
- 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 | 995666 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24689-146-01 | Meclizine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24689-146 | MECLIZINE HYDROCHLORIDE TABLET [APNAR PHARMA LP] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250112_ed43bf21-f3da-245c-e053-2995a90a504c.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 |
|---|
| 24689-146-01 | 24689014601 | 100 TABLET in 1 BOTTLE (24689-146-01) | 100 tablet | 2022-11-21 | 0000-00-00 | No | No | Current |