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Cetirizine
Cetirizine - 21695-878-04 - (Cetirizine)
Drug Information of Cetirizine
| Product NDC: | 21695-878 |
| Proprietary Name: | Cetirizine |
| Non Proprietary Name: | Cetirizine |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Cetirizine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cetirizine
| Product NDC: | 21695-878 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078398 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080617 |
Package Information of Cetirizine
| Package NDC: | 21695-878-04 |
| Package Description: | 120 mL in 1 BOTTLE (21695-878-04) |
NDC Information of Cetirizine
| NDC Code | 21695-878-04 |
| Proprietary Name | Cetirizine |
| Package Description | 120 mL in 1 BOTTLE (21695-878-04) |
| Product NDC | 21695-878 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080617 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
