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Diphenhydramine Hydrochloride
Diphenhydramine Hydrochloride - 49349-836-41 - (diphenhydramine hydrochloride)
Drug Information of Diphenhydramine Hydrochloride
| Product NDC: | 49349-836 |
| Proprietary Name: | Diphenhydramine Hydrochloride |
| Non Proprietary Name: | diphenhydramine hydrochloride |
| Active Ingredient(s): | 50 mg/mL & nbsp; diphenhydramine hydrochloride |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine Hydrochloride
| Product NDC: | 49349-836 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080817 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130613 |
Package Information of Diphenhydramine Hydrochloride
| Package NDC: | 49349-836-41 |
| Package Description: | 1 mL in 1 VIAL (49349-836-41) |
NDC Information of Diphenhydramine Hydrochloride
| NDC Code | 49349-836-41 |
| Proprietary Name | Diphenhydramine Hydrochloride |
| Package Description | 1 mL in 1 VIAL (49349-836-41) |
| Product NDC | 49349-836 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diphenhydramine hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20130613 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
