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Benadryl
Benadryl - 21695-811-24 - (Diphenhydramine Hydrochloride)
Drug Information of Benadryl
| Product NDC: | 21695-811 |
| Proprietary Name: | Benadryl |
| 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) |
Labeler Information of Benadryl
| Product NDC: | 21695-811 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090101 |
Package Information of Benadryl
| Package NDC: | 21695-811-24 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (21695-811-24) > 8 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Benadryl
| NDC Code | 21695-811-24 |
| Proprietary Name | Benadryl |
| Package Description | 3 BLISTER PACK in 1 CARTON (21695-811-24) > 8 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 21695-811 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
