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NDC 68788-7873-01 Meclizine Hydrochloride 25 mg/1 Details
Meclizine Hydrochloride 25 mg/1
Meclizine Hydrochloride is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. 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: 68788-7873-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Meclizine
Product Information
| NDC | 68788-7873 |
|---|---|
| Product ID | 68788-7873_a0a09bcd-2b4e-4a65-a9ee-a255ee423ffa |
| 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 | Meclizine Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Meclizine Hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, CHEWABLE |
| Route | ORAL |
| Active Ingredient Strength | 25 |
| Active Ingredient Units | mg/1 |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Labeler Name | Preferred Pharmaceuticals Inc. |
| Pharmaceutical Class | Antiemetic [EPC], Emesis Suppression [PE] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part336 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68788-7873-01 (68788787301)
| NDC Package Code | 68788-7873-1 |
|---|---|
| Billing NDC | 68788787301 |
| Package | 100 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-1) |
| Marketing Start Date | 2021-02-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |