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Diphenhydramine Hydrochloride
Diphenhydramine Hydrochloride - 51079-066-19 - (Diphenhydramine Hydrochloride)
Drug Information of Diphenhydramine Hydrochloride
| Product NDC: | 51079-066 |
| Proprietary Name: | Diphenhydramine Hydrochloride |
| 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 Hydrochloride
| Product NDC: | 51079-066 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080738 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110823 |
Package Information of Diphenhydramine Hydrochloride
| Package NDC: | 51079-066-19 |
| Package Description: | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-066-19) > 1 CAPSULE in 1 BLISTER PACK (51079-066-17) |
NDC Information of Diphenhydramine Hydrochloride
| NDC Code | 51079-066-19 |
| Proprietary Name | Diphenhydramine Hydrochloride |
| Package Description | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-066-19) > 1 CAPSULE in 1 BLISTER PACK (51079-066-17) |
| Product NDC | 51079-066 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110823 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
