Product NDC: | 63548-3482 |
Proprietary Name: | Diphenhydramine Hydrochloride |
Non Proprietary Name: | Diphenhydramine Hydrochloride |
Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63548-3482 |
Labeler Name: | Avema Pharma Solutions |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100102 |
Package NDC: | 63548-3482-1 |
Package Description: | 24 TABLET, COATED in 1 BLISTER PACK (63548-3482-1) |
NDC Code | 63548-3482-1 |
Proprietary Name | Diphenhydramine Hydrochloride |
Package Description | 24 TABLET, COATED in 1 BLISTER PACK (63548-3482-1) |
Product NDC | 63548-3482 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine Hydrochloride |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20100102 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Avema Pharma Solutions |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |