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Cetirizine HCl
Cetirizine HCl - 49738-211-25 - (Cetirizine Hydrochloride)
Drug Information of Cetirizine HCl
| Product NDC: | 49738-211 |
| Proprietary Name: | Cetirizine HCl |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cetirizine HCl
| Product NDC: | 49738-211 |
| Labeler Name: | SMART SENSE (Kmart) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022429 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130501 |
Package Information of Cetirizine HCl
| Package NDC: | 49738-211-25 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 PACKAGE (49738-211-25) > 25 CAPSULE in 1 BOTTLE, PLASTIC |
NDC Information of Cetirizine HCl
| NDC Code | 49738-211-25 |
| Proprietary Name | Cetirizine HCl |
| Package Description | 1 BOTTLE, PLASTIC in 1 PACKAGE (49738-211-25) > 25 CAPSULE in 1 BOTTLE, PLASTIC |
| Product NDC | 49738-211 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130501 |
| Marketing Category Name | NDA |
| Labeler Name | SMART SENSE (Kmart) |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
