Product NDC: | 54838-135 |
Proprietary Name: | Siladryl Allergy Medicine |
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) |
Product NDC: | 54838-135 |
Labeler Name: | Silarx Pharmaceuticals, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19970101 |
Package NDC: | 54838-135-70 |
Package Description: | 237 mL in 1 BOTTLE (54838-135-70) |
NDC Code | 54838-135-70 |
Proprietary Name | Siladryl Allergy Medicine |
Package Description | 237 mL in 1 BOTTLE (54838-135-70) |
Product NDC | 54838-135 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | diphenhydramine hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19970101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Silarx Pharmaceuticals, Inc |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 12.5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |