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Diphenhydramine Hydrochloride
Diphenhydramine Hydrochloride - 76045-102-10 - (Diphenhydramine Hydrochloride)
Drug Information of Diphenhydramine Hydrochloride
| Product NDC: | 76045-102 |
| Proprietary Name: | Diphenhydramine Hydrochloride |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 50 mg/mL & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine Hydrochloride
| Product NDC: | 76045-102 |
| Labeler Name: | BD Rx Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091526 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130408 |
Package Information of Diphenhydramine Hydrochloride
| Package NDC: | 76045-102-10 |
| Package Description: | 24 BLISTER PACK in 1 CARTON (76045-102-10) > 1 SYRINGE, GLASS in 1 BLISTER PACK > 1 mL in 1 SYRINGE, GLASS |
NDC Information of Diphenhydramine Hydrochloride
| NDC Code | 76045-102-10 |
| Proprietary Name | Diphenhydramine Hydrochloride |
| Package Description | 24 BLISTER PACK in 1 CARTON (76045-102-10) > 1 SYRINGE, GLASS in 1 BLISTER PACK > 1 mL in 1 SYRINGE, GLASS |
| Product NDC | 76045-102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20130408 |
| Marketing Category Name | ANDA |
| Labeler Name | BD Rx Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
