Home
>
National Drug Code (NDC)
>
Cetirizine
Cetirizine - 75921-402-30 - (Cetirizine Hydrochloride)
Drug Information of Cetirizine
| Product NDC: | 75921-402 |
| Proprietary Name: | Cetirizine |
| 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
| Product NDC: | 75921-402 |
| Labeler Name: | Life Line Home Care Services, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077829 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120203 |
Package Information of Cetirizine
| Package NDC: | 75921-402-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (75921-402-30) |
NDC Information of Cetirizine
| NDC Code | 75921-402-30 |
| Proprietary Name | Cetirizine |
| Package Description | 30 TABLET in 1 BOTTLE (75921-402-30) |
| Product NDC | 75921-402 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120203 |
| Marketing Category Name | ANDA |
| Labeler Name | Life Line Home Care Services, Inc. |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
