Package 50090-0878-0
Brand: diphenhydramine hydrochloride
Generic: diphenhydramine hydrochloridePackage Facts
Identity
Package NDC
50090-0878-0
Digits Only
5009008780
Product NDC
50090-0878
Description
1 VIAL in 1 CARTON (50090-0878-0) / 50 mL in 1 VIAL
Marketing
Marketing Status
Brand
diphenhydramine hydrochloride
Generic
diphenhydramine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "237e3d41-c0d2-424c-8d47-9ebd833b99fe", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["eedb421c-0020-4e5f-8b09-26a1cbabb681"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (50090-0878-0) / 50 mL in 1 VIAL", "package_ndc": "50090-0878-0", "marketing_start_date": "20141128"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "50090-0878_237e3d41-c0d2-424c-8d47-9ebd833b99fe", "dosage_form": "INJECTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-0878", "generic_name": "diphenhydramine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA080817", "marketing_category": "ANDA", "marketing_start_date": "19721127", "listing_expiration_date": "20261231"}