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NDC 65197-0520-16 BONINE MAX 50 mg/1 Details
BONINE MAX 50 mg/1
BONINE MAX is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by WellSpring Pharmaceutical Corporation. 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: 65197-0520-16Last Updated: 04/28/2024
MedLinePlus Full Drug Details: Meclizine
Product Information
| NDC | 65197-0520 |
|---|---|
| Product ID | 65197-520_2b84f935-afef-4caa-a93b-fd42cdc6375b |
| 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 | BONINE MAX |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | meclizine hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, CHEWABLE |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/1 |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Labeler Name | WellSpring Pharmaceutical Corporation |
| 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 65197-0520-16 (65197052016)
| NDC Package Code | 65197-520-16 |
|---|---|
| Billing NDC | 65197052016 |
| Package | 2 BLISTER PACK in 1 BOX (65197-520-16) / 8 TABLET, CHEWABLE in 1 BLISTER PACK |
| Marketing Start Date | 2023-03-24 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |