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Cetirizine Hydrochloride
Cetirizine Hydrochloride - 21695-709-30 - (Cetirizine Hydrochloride)
Drug Information of Cetirizine Hydrochloride
| Product NDC: | 21695-709 |
| 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: | 21695-709 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077946 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071227 |
Package Information of Cetirizine Hydrochloride
| Package NDC: | 21695-709-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (21695-709-30) |
NDC Information of Cetirizine Hydrochloride
| NDC Code | 21695-709-30 |
| Proprietary Name | Cetirizine Hydrochloride |
| Package Description | 30 TABLET in 1 BOTTLE (21695-709-30) |
| Product NDC | 21695-709 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20071227 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
