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Diphenhydramine
Diphenhydramine - 52959-053-52 - (Diphenhydramine Hydrochloride)
Drug Information of Diphenhydramine
| Product NDC: | 52959-053 |
| Proprietary Name: | Diphenhydramine |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine
| Product NDC: | 52959-053 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110817 |
Package Information of Diphenhydramine
| Package NDC: | 52959-053-52 |
| Package Description: | 52 CAPSULE in 1 BOTTLE (52959-053-52) |
NDC Information of Diphenhydramine
| NDC Code | 52959-053-52 |
| Proprietary Name | Diphenhydramine |
| Package Description | 52 CAPSULE in 1 BOTTLE (52959-053-52) |
| Product NDC | 52959-053 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110817 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
