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Zentrip
Zentrip - 49873-803-01 - (meclizine hydrochloride)
Drug Information of Zentrip
| Product NDC: | 49873-803 |
| Proprietary Name: | Zentrip |
| Non Proprietary Name: | meclizine hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; meclizine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | FILM, SOLUBLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zentrip
| Product NDC: | 49873-803 |
| Labeler Name: | Sato Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090203 |
Package Information of Zentrip
| Package NDC: | 49873-803-01 |
| Package Description: | 8 PACKET in 1 CARTON (49873-803-01) > 1 FILM, SOLUBLE in 1 PACKET |
NDC Information of Zentrip
| NDC Code | 49873-803-01 |
| Proprietary Name | Zentrip |
| Package Description | 8 PACKET in 1 CARTON (49873-803-01) > 1 FILM, SOLUBLE in 1 PACKET |
| Product NDC | 49873-803 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | meclizine hydrochloride |
| Dosage Form Name | FILM, SOLUBLE |
| Route Name | ORAL |
| Start Marketing Date | 20090203 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sato Pharmaceutical Co., Ltd. |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
