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sunmark childrens all day allergy
sunmark childrens all day allergy - 49348-934-34 - (cetirizine Hydrochloride)
Drug Information of sunmark childrens all day allergy
| Product NDC: | 49348-934 |
| Proprietary Name: | sunmark childrens all day allergy |
| Non Proprietary Name: | cetirizine Hydrochloride |
| Active Ingredient(s): | 5 mg/5mL & nbsp; cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark childrens all day allergy
| Product NDC: | 49348-934 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090254 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100909 |
Package Information of sunmark childrens all day allergy
| Package NDC: | 49348-934-34 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-934-34) > 118 mL in 1 BOTTLE |
NDC Information of sunmark childrens all day allergy
| NDC Code | 49348-934-34 |
| Proprietary Name | sunmark childrens all day allergy |
| Package Description | 1 BOTTLE in 1 CARTON (49348-934-34) > 118 mL in 1 BOTTLE |
| Product NDC | 49348-934 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | cetirizine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100909 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
