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Childrens Benadryl Allergy
Childrens Benadryl Allergy - 50580-334-10 - (Diphenhydramine Hydrochloride)
Drug Information of Childrens Benadryl Allergy
| Product NDC: | 50580-334 |
| 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): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Childrens Benadryl Allergy
| Product NDC: | 50580-334 |
| 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: | 20081201 |
Package Information of Childrens Benadryl Allergy
| Package NDC: | 50580-334-10 |
| Package Description: | 10 POUCH in 1 CARTON (50580-334-10) > 5 mL in 1 POUCH |
NDC Information of Childrens Benadryl Allergy
| NDC Code | 50580-334-10 |
| Proprietary Name | Childrens Benadryl Allergy |
| Package Description | 10 POUCH in 1 CARTON (50580-334-10) > 5 mL in 1 POUCH |
| Product NDC | 50580-334 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20081201 |
| 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 |
