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Cetirizine hydrochloride
Cetirizine hydrochloride - 68752-005-90 - (Cetirizine hydrochloride)
Drug Information of Cetirizine hydrochloride
| Product NDC: | 68752-005 |
| Proprietary Name: | Cetirizine hydrochloride |
| Non Proprietary Name: | Cetirizine hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cetirizine hydrochloride
| Product NDC: | 68752-005 |
| Labeler Name: | TriMarc Labs |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077498 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100625 |
Package Information of Cetirizine hydrochloride
| Package NDC: | 68752-005-90 |
| Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (68752-005-90) |
NDC Information of Cetirizine hydrochloride
| NDC Code | 68752-005-90 |
| Proprietary Name | Cetirizine hydrochloride |
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (68752-005-90) |
| Product NDC | 68752-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100625 |
| Marketing Category Name | ANDA |
| Labeler Name | TriMarc Labs |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
