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NAUS-EASE
NAUS-EASE - 49467-124-16 - (MECLIZINE HYDROCHLORIDE)
Drug Information of NAUS-EASE
| Product NDC: | 49467-124 |
| Proprietary Name: | NAUS-EASE |
| Non Proprietary Name: | MECLIZINE HYDROCHLORIDE |
| Active Ingredient(s): | 25 mg/1 & nbsp; MECLIZINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NAUS-EASE
| Product NDC: | 49467-124 |
| Labeler Name: | Sunascen Therapeutics LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA040659 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120416 |
Package Information of NAUS-EASE
| Package NDC: | 49467-124-16 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (49467-124-16) > 8 TABLET in 1 BLISTER PACK |
NDC Information of NAUS-EASE
| NDC Code | 49467-124-16 |
| Proprietary Name | NAUS-EASE |
| Package Description | 2 BLISTER PACK in 1 CARTON (49467-124-16) > 8 TABLET in 1 BLISTER PACK |
| Product NDC | 49467-124 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MECLIZINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120416 |
| Marketing Category Name | ANDA |
| Labeler Name | Sunascen Therapeutics LLC |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
