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MECLIZINE HYDROCHLORIDE
MECLIZINE HYDROCHLORIDE - 52959-033-10 - (Meclizine Hydrocloride)
Drug Information of MECLIZINE HYDROCHLORIDE
| Product NDC: | 52959-033 |
| Proprietary Name: | MECLIZINE HYDROCHLORIDE |
| Non Proprietary Name: | Meclizine Hydrocloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Meclizine Hydrocloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MECLIZINE HYDROCHLORIDE
| Product NDC: | 52959-033 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040659 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100604 |
Package Information of MECLIZINE HYDROCHLORIDE
| Package NDC: | 52959-033-10 |
| Package Description: | 10 TABLET in 1 BOTTLE (52959-033-10) |
NDC Information of MECLIZINE HYDROCHLORIDE
| NDC Code | 52959-033-10 |
| Proprietary Name | MECLIZINE HYDROCHLORIDE |
| Package Description | 10 TABLET in 1 BOTTLE (52959-033-10) |
| Product NDC | 52959-033 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Meclizine Hydrocloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100604 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiemetic [EPC],Emesis Suppression [PE] |
