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Diphenhydramine
Diphenhydramine - 21695-304-24 - (Diphenhydramine)
Drug Information of Diphenhydramine
| Product NDC: | 21695-304 |
| Proprietary Name: | Diphenhydramine |
| Non Proprietary Name: | Diphenhydramine |
| Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine
| Product NDC: | 21695-304 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20070101 |
Package Information of Diphenhydramine
| Package NDC: | 21695-304-24 |
| Package Description: | 24 CAPSULE in 1 BOTTLE (21695-304-24) |
NDC Information of Diphenhydramine
| NDC Code | 21695-304-24 |
| Proprietary Name | Diphenhydramine |
| Package Description | 24 CAPSULE in 1 BOTTLE (21695-304-24) |
| Product NDC | 21695-304 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20070101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
