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SunMark All Day Allergy
SunMark All Day Allergy - 49348-843-34 - (cetirizine hydrochloride)
Drug Information of SunMark All Day Allergy
| Product NDC: | 49348-843 |
| Proprietary Name: | SunMark 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 All Day Allergy
| Product NDC: | 49348-843 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090254 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080423 |
Package Information of SunMark All Day Allergy
| Package NDC: | 49348-843-34 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-843-34) > 120 mL in 1 BOTTLE |
NDC Information of SunMark All Day Allergy
| NDC Code | 49348-843-34 |
| Proprietary Name | SunMark All Day Allergy |
| Package Description | 1 BOTTLE in 1 CARTON (49348-843-34) > 120 mL in 1 BOTTLE |
| Product NDC | 49348-843 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | cetirizine hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080423 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
