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All Day Allergy
All Day Allergy - 59726-220-14 - (Cetirizine HCl)
Drug Information of All Day Allergy
| Product NDC: | 59726-220 |
| Proprietary Name: | All Day Allergy |
| Non Proprietary Name: | Cetirizine HCl |
| Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of All Day Allergy
| Product NDC: | 59726-220 |
| Labeler Name: | P and L Development of New York Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078427 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121205 |
Package Information of All Day Allergy
| Package NDC: | 59726-220-14 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59726-220-14) > 14 TABLET in 1 BLISTER PACK |
NDC Information of All Day Allergy
| NDC Code | 59726-220-14 |
| Proprietary Name | All Day Allergy |
| Package Description | 1 BLISTER PACK in 1 CARTON (59726-220-14) > 14 TABLET in 1 BLISTER PACK |
| Product NDC | 59726-220 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121205 |
| Marketing Category Name | ANDA |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
