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Cetirizine HCL 10 mg All Day Allergy Relief
Cetirizine HCL 10 mg All Day Allergy Relief - 55315-129-30 - (Cetirizine Hydrochloride)
Drug Information of Cetirizine HCL 10 mg All Day Allergy Relief
| Product NDC: | 55315-129 |
| Proprietary Name: | Cetirizine HCL 10 mg All Day Allergy Relief |
| 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 Cetirizine HCL 10 mg All Day Allergy Relief
| Product NDC: | 55315-129 |
| Labeler Name: | Freds Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078780 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130301 |
Package Information of Cetirizine HCL 10 mg All Day Allergy Relief
| Package NDC: | 55315-129-30 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (55315-129-30) > 15 TABLET in 1 BLISTER PACK |
NDC Information of Cetirizine HCL 10 mg All Day Allergy Relief
| NDC Code | 55315-129-30 |
| Proprietary Name | Cetirizine HCL 10 mg All Day Allergy Relief |
| Package Description | 2 BLISTER PACK in 1 CARTON (55315-129-30) > 15 TABLET in 1 BLISTER PACK |
| Product NDC | 55315-129 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | ANDA |
| Labeler Name | Freds Inc |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
