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NDC 51655-0175-52 Meclizine Hydrochloride 25 mg/1 Details
Meclizine Hydrochloride 25 mg/1
Meclizine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. 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: 51655-0175-52Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Meclizine
Product Information
| NDC | 51655-0175 |
|---|---|
| Product ID | 51655-175_f2b4716c-411b-62cd-e053-2a95a90a6f4b |
| 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 PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 25 |
| Active Ingredient Units | mg/1 |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Labeler Name | Northwind Pharmaceuticals, LLC |
| Pharmaceutical Class | Antiemetic [EPC], Emesis Suppression [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA201451 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 51655-0175-52 (51655017552)
| NDC Package Code | 51655-175-52 |
|---|---|
| Billing NDC | 51655017552 |
| Package | 30 TABLET in 1 BOTTLE, PLASTIC (51655-175-52) |
| Marketing Start Date | 2022-10-07 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |