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Cetirizine Hydrochloride
Cetirizine Hydrochloride - 0536-4088-07 - (Cetirizine)
Drug Information of Cetirizine Hydrochloride
| Product NDC: | 0536-4088 |
| Proprietary Name: | Cetirizine Hydrochloride |
| Non Proprietary Name: | Cetirizine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cetirizine Hydrochloride
| Product NDC: | 0536-4088 |
| Labeler Name: | Rugby Laboratories Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078780 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120323 |
Package Information of Cetirizine Hydrochloride
| Package NDC: | 0536-4088-07 |
| Package Description: | 2 BLISTER PACK in 1 BOX (0536-4088-07) > 30 TABLET in 1 BLISTER PACK |
NDC Information of Cetirizine Hydrochloride
| NDC Code | 0536-4088-07 |
| Proprietary Name | Cetirizine Hydrochloride |
| Package Description | 2 BLISTER PACK in 1 BOX (0536-4088-07) > 30 TABLET in 1 BLISTER PACK |
| Product NDC | 0536-4088 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120323 |
| Marketing Category Name | ANDA |
| Labeler Name | Rugby Laboratories Inc |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
