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All Day
All Day - 46122-101-26 - (Cetirizine Hydrochloride)
Drug Information of All Day
| Product NDC: | 46122-101 |
| Proprietary Name: | All Day |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of All Day
| Product NDC: | 46122-101 |
| Labeler Name: | Amerisource Bergen |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA201546 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110520 |
Package Information of All Day
| Package NDC: | 46122-101-26 |
| Package Description: | 1 BOTTLE in 1 CARTON (46122-101-26) > 118 mL in 1 BOTTLE |
NDC Information of All Day
| NDC Code | 46122-101-26 |
| Proprietary Name | All Day |
| Package Description | 1 BOTTLE in 1 CARTON (46122-101-26) > 118 mL in 1 BOTTLE |
| Product NDC | 46122-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20110520 |
| Marketing Category Name | ANDA |
| Labeler Name | Amerisource Bergen |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
