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Bonine
Bonine - 63736-124-16 - (meclizine hydrochloride)
Drug Information of Bonine
| Product NDC: | 63736-124 |
| Proprietary Name: | Bonine |
| Non Proprietary Name: | meclizine hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; meclizine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bonine
| Product NDC: | 63736-124 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090608 |
Package Information of Bonine
| Package NDC: | 63736-124-16 |
| Package Description: | 16 TABLET, CHEWABLE in 1 BOX (63736-124-16) |
NDC Information of Bonine
| NDC Code | 63736-124-16 |
| Proprietary Name | Bonine |
| Package Description | 16 TABLET, CHEWABLE in 1 BOX (63736-124-16) |
| Product NDC | 63736-124 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | meclizine hydrochloride |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20090608 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
