Package 83939-0008-4
Brand: m-dryl
Generic: diphenhydramine hydrochloridePackage Facts
Identity
Package NDC
83939-0008-4
Digits Only
8393900084
Product NDC
83939-0008
Description
50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (83939-0008-4) / 5 mL in 1 CUP, UNIT-DOSE
Marketing
Marketing Status
Brand
m-dryl
Generic
diphenhydramine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42a0e590-e444-2058-e063-6294a90af461", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049906"], "spl_set_id": ["42a0e577-a1b6-2c16-e063-6294a90af8e3"], "manufacturer_name": ["VERITYRX, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 CUP, UNIT-DOSE (83939-0008-1)", "package_ndc": "83939-0008-1", "marketing_start_date": "20251110"}, {"sample": false, "description": "10 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (83939-0008-2) / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "83939-0008-2", "marketing_start_date": "20251110"}, {"sample": false, "description": "40 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (83939-0008-3) / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "83939-0008-3", "marketing_start_date": "20251110"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (83939-0008-4) / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "83939-0008-4", "marketing_start_date": "20251110"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 BOTTLE, UNIT-DOSE (83939-0008-5) / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "83939-0008-5", "marketing_start_date": "20251110"}], "brand_name": "M-Dryl", "product_id": "83939-0008_42a0e590-e444-2058-e063-6294a90af461", "dosage_form": "LIQUID", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "83939-0008", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "VERITYRX, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "M-Dryl", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}