Product NDC: | 67046-126 |
Proprietary Name: | DIPHENDYDRAMINE HYDROCHLORIDE |
Non Proprietary Name: | DIPHENDYDRAMINE HYDROCHLORIDE |
Active Ingredient(s): | 50 mg/1 & nbsp; DIPHENDYDRAMINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67046-126 |
Labeler Name: | Contract Pharmacy Services-PA |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part345 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100805 |
Package NDC: | 67046-126-30 |
Package Description: | 30 CAPSULE in 1 BLISTER PACK (67046-126-30) |
NDC Code | 67046-126-30 |
Proprietary Name | DIPHENDYDRAMINE HYDROCHLORIDE |
Package Description | 30 CAPSULE in 1 BLISTER PACK (67046-126-30) |
Product NDC | 67046-126 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DIPHENDYDRAMINE HYDROCHLORIDE |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20100805 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Contract Pharmacy Services-PA |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes |