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Diphenhydramine Hydrochloride
Diphenhydramine Hydrochloride - 51079-967-19 - (diphenhydramine hydrochloride)
Drug Information of Diphenhydramine Hydrochloride
| Product NDC: | 51079-967 |
| Proprietary Name: | Diphenhydramine Hydrochloride |
| Non Proprietary Name: | diphenhydramine hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; diphenhydramine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine Hydrochloride
| Product NDC: | 51079-967 |
| Labeler Name: | UDL Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110614 |
Package Information of Diphenhydramine Hydrochloride
| Package NDC: | 51079-967-19 |
| Package Description: | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-967-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-967-17) |
NDC Information of Diphenhydramine Hydrochloride
| NDC Code | 51079-967-19 |
| Proprietary Name | Diphenhydramine Hydrochloride |
| Package Description | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-967-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-967-17) |
| Product NDC | 51079-967 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110614 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | UDL Laboratories Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
