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Zero Allergy
Zero Allergy - 58593-827-14 - (Cetirizine Hydrochloride)
Drug Information of Zero Allergy
| Product NDC: | 58593-827 |
| Proprietary Name: | Zero Allergy |
| 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 Zero Allergy
| Product NDC: | 58593-827 |
| Labeler Name: | Efficient Laboratories Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077498 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130401 |
Package Information of Zero Allergy
| Package NDC: | 58593-827-14 |
| Package Description: | 14 TABLET in 1 BLISTER PACK (58593-827-14) |
NDC Information of Zero Allergy
| NDC Code | 58593-827-14 |
| Proprietary Name | Zero Allergy |
| Package Description | 14 TABLET in 1 BLISTER PACK (58593-827-14) |
| Product NDC | 58593-827 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130401 |
| Marketing Category Name | ANDA |
| Labeler Name | Efficient Laboratories Inc |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
