Product NDC: | 57664-263 |
Proprietary Name: | CETIRIZINE HYDROLORIDE Allergy |
Non Proprietary Name: | CETIRIZINE HYDROLORIDE |
Active Ingredient(s): | 1 mg/mL & nbsp; CETIRIZINE HYDROLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57664-263 |
Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA091327 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111201 |
Package NDC: | 57664-263-34 |
Package Description: | 470 mL in 1 BOTTLE (57664-263-34) |
NDC Code | 57664-263-34 |
Proprietary Name | CETIRIZINE HYDROLORIDE Allergy |
Package Description | 470 mL in 1 BOTTLE (57664-263-34) |
Product NDC | 57664-263 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CETIRIZINE HYDROLORIDE |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20111201 |
Marketing Category Name | ANDA |
Labeler Name | Caraco Pharmaceutical Laboratories, Ltd |
Substance Name | CETIRIZINE HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes |