Motion Sickness Relief
- Product NDC
- 50844-403
- 11-digit product format
- 508440403
- Labeler code
- 50844
- Product ID
- 50844-403_f66f3f18-c6ac-4e55-a162-fcba30e5e282
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- L.N.K. International, Inc.
- Application
- part336
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2002-06-24
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC], Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50844-403-19 | Motion Sickness Relief | 8 in 1 BLISTER PACK | TABLET | 8 | | 15 |
| 50844-403-19 | Motion Sickness Relief | 1 in 1 CARTON | TABLET | 1 | | 15 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50844-403 | MOTION SICKNESS RELIEF (MECLIZINE HCL) TABLET [L.N.K. INTERNATIONAL, INC.] | 14 | Legacy NDC, 2 package rows | 20240711_8e1889de-fbef-44f1-bbfb-c68a78e6330c.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 |
|---|
| 50844-403-19 | 50844040319 | 1 BLISTER PACK in 1 CARTON (50844-403-19) > 8 TABLET in 1 BLISTER PACK | 1 blister pack | 2002-06-24 | 0000-00-00 | No | No | Current |