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
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Meclizine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MECLIZINE HYDROCHLORIDE | 25 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| HDP7W44CIO | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 995666 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| ed43bf21-f3da-245c-e053-2995a90a504c | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| ac6963c4-31c6-325f-ee58-83a0a06597ad | Product name | 5 | 20221206 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 24689-146-01 | Meclizine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | 2 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 24689-146-01 | EA - Each | 24689-146 | 3e171323-9e53-4ba0-b1a2-09648d23e598 | 1 | 2023-02-06 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Meclizine Hydrochloride | MECLIZINE HYDROCHLORIDE | NuCare Pharmaceuticals,Inc. | d0d8b376-8fe9-8776-e053-2a95a90ae651 | 2026-01-27 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 4f806804-48c7-414e-a177-5d3daf5b22e3 | 2026-01-20 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | United Natural Foods, Inc. dba UNFI | 108bb943-529f-4510-b770-b54eca493ae0 | 2026-01-12 | Warnings | M009 |
| Less Drowsy Motion Sickness Relief | MECLIZINE HCL | Rite Aid Corporation | 2f9ebe6b-ffde-41de-9eaa-b03d87d33005 | 2026-01-09 | Warnings | M009 |
| Motion Sickness Relief | DIMENHYDRINATE | Rite Aid Corporation | 4f532984-aeee-4dde-972c-742bdf12868f | 2026-01-07 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | Family Dollar Services Inc | e34126e3-52ef-4999-bf61-cba9b1818259 | 2026-01-05 | Warnings | M009 |
| CVS Motion Sickness Fast Melting | MECLIZINE HYDROCHLORIDE | CVS Pharmacy, Inc. | 2a723bce-a581-4558-b028-22f1f9125dd5 | 2025-12-30 | Warnings | M009 |
| Wal-Dram 2 Quick-Dissolving | MECLIZINE HYDROCHLORIDE | Walgreen Co. | f3116203-1b8f-438a-b779-7bdd90eaf79e | 2025-12-30 | Warnings | M009 |
| MECLIZINE | MECLIZINE HCL 12.5 MG | Pharbest Pharmaceuticals, Inc. | 8b3c9283-b618-4d57-9f15-7cf73e8737f5 | 2025-12-24 | Warnings | M009 |
| MECLIZINE | MECLIZINE HCL 25MG | Pharbest Pharmaceuticals, Inc. | 4bac2765-045c-405e-8006-8c5cfdfa89bc | 2025-12-24 | Warnings | M009 |
| DRAMAMINE | MECLIZINE HYDROCHLORIDE | Medtech Products Inc. | fdcbcc4e-9370-4975-8905-1f12c73fdc8c | 2025-12-23 | Warnings | M009 |
| DRAMAMINE | MECLIZINE HYDROCHLORIDE | Medtech Products Inc. | 3a960d43-62aa-464e-92b9-d83042ba02bf | 2025-12-23 | Warnings | M009 |
| DRAMAMINE | MECLIZINE HYDROCHLORIDE | Medtech Products Inc. | 6efd3473-ee14-4ee0-8a58-d15a64a9224a | 2025-12-18 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | Rite Aid Corporation | e599dc64-ac10-4f4e-9318-e9fab0526488 | 2025-11-15 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | Kroger Company | 64e0496c-5e09-46e9-94b9-624163d71b60 | 2025-11-05 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | Walgreen Company | 27bd9c74-c85e-4eeb-9e43-4120f9001187 | 2025-11-05 | Warnings | M009 |
| Dramamine Original Formula | DIMENHYDRINATE | Medtech Products Inc. | f9302a5a-295a-4501-9332-e3f5eb387362 | 2025-10-23 | Warnings | M009 |
| Meclizine Hydrochloride | MECLIZINE HYDROCHLORIDE | CVS Pharmacy, Inc | b57fc6c2-fbfc-24c3-e053-2995a90a3389 | 2025-10-16 | Warnings | M009 |
| Motion Sickness Relief | MECLIZINE HCL | Amerisource Bergen | 503f62e7-8ec8-4409-9697-4efef4ff7b15 | 2025-10-08 | Warnings | M009 |
| Meclizine HCL 25 mg | MECLIZINE HCL | Proficient Rx LP | d08fa6f5-4293-4468-814e-7dccbd281209 | 2025-10-01 | Warnings | M009 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 995666 | meclizine HCl 25 MG Oral Tablet | PSN | ed43bf21-f3da-245c-e053-2995a90a504c | 2 |
| 995666 | meclizine hydrochloride 25 MG Oral Tablet | SCD | ed43bf21-f3da-245c-e053-2995a90a504c | 2 |
Packages#
| 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 |