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NDC 49873-0805-01 ZenTrip Motion Sickness 25 mg/1 Details
ZenTrip Motion Sickness 25 mg/1
ZenTrip Motion Sickness is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Sato Pharmaceutical Co., LTD. The primary component is MECLIZINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Meclizine is used to prevent and treat nausea, vomiting, and dizziness caused by motion sickness. It is most effective if taken before symptoms appear.
Related Packages: 49873-0805-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Meclizine
Product Information
| NDC | 49873-0805 |
|---|---|
| Product ID | 49873-805_0949e5cb-b9e4-cee1-e063-6394a90a5377 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | ZenTrip Motion Sickness |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Meclizine Hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 25 |
| Active Ingredient Units | mg/1 |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Labeler Name | Sato Pharmaceutical Co., LTD |
| Pharmaceutical Class | Antiemetic [EPC], Emesis Suppression [PE] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M009 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 49873-0805-01 (49873080501)
| NDC Package Code | 49873-805-01 |
|---|---|
| Billing NDC | 49873080501 |
| Package | 2 BLISTER PACK in 1 BOX (49873-805-01) / 6 TABLET in 1 BLISTER PACK |
| Marketing Start Date | 2021-05-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |