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DiphenhydrAMINE Hydrochloride
DiphenhydrAMINE Hydrochloride - 0409-2290-31 - (DIPHENHYDRAMINE HYDROCHLORIDE)
Drug Information of DiphenhydrAMINE Hydrochloride
| Product NDC: | 0409-2290 |
| Proprietary Name: | DiphenhydrAMINE Hydrochloride |
| Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 50 mg/mL & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DiphenhydrAMINE Hydrochloride
| Product NDC: | 0409-2290 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040140 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19881120 |
Package Information of DiphenhydrAMINE Hydrochloride
| Package NDC: | 0409-2290-31 |
| Package Description: | 10 CARTRIDGE in 1 BOX (0409-2290-31) > 1 mL in 1 CARTRIDGE |
NDC Information of DiphenhydrAMINE Hydrochloride
| NDC Code | 0409-2290-31 |
| Proprietary Name | DiphenhydrAMINE Hydrochloride |
| Package Description | 10 CARTRIDGE in 1 BOX (0409-2290-31) > 1 mL in 1 CARTRIDGE |
| Product NDC | 0409-2290 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19881120 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
