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Cetirizine Hydrochloride
Cetirizine Hydrochloride - 57664-541-27 - (Cetirizine Hydrochloride)
Drug Information of Cetirizine Hydrochloride
| Product NDC: | 57664-541 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cetirizine Hydrochloride
| Product NDC: | 57664-541 |
| Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077499 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071227 |
Package Information of Cetirizine Hydrochloride
| Package NDC: | 57664-541-27 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (57664-541-27) |
NDC Information of Cetirizine Hydrochloride
| NDC Code | 57664-541-27 |
| Proprietary Name | Cetirizine Hydrochloride |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (57664-541-27) |
| Product NDC | 57664-541 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20071227 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories, Ltd. |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
