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Childrens Benadryl ALLERGY
Childrens Benadryl ALLERGY - 50580-534-04 - (Diphenhydramine hydrochloride)
Drug Information of Childrens Benadryl ALLERGY
| Product NDC: | 50580-534 |
| Proprietary Name: | Childrens Benadryl ALLERGY |
| Non Proprietary Name: | Diphenhydramine hydrochloride |
| Active Ingredient(s): | 12.5 mg/5mL & nbsp; Diphenhydramine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Childrens Benadryl ALLERGY
| Product NDC: | 50580-534 |
| Labeler Name: | McNeil Consumer Healthcare Div. McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080701 |
Package Information of Childrens Benadryl ALLERGY
| Package NDC: | 50580-534-04 |
| Package Description: | 1 BOTTLE in 1 CARTON (50580-534-04) > 118 mL in 1 BOTTLE |
NDC Information of Childrens Benadryl ALLERGY
| NDC Code | 50580-534-04 |
| Proprietary Name | Childrens Benadryl ALLERGY |
| Package Description | 1 BOTTLE in 1 CARTON (50580-534-04) > 118 mL in 1 BOTTLE |
| Product NDC | 50580-534 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20080701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McNeil Consumer Healthcare Div. McNeil-PPC, Inc |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 12.5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
