Package 63323-664-16

Brand: diphenhydramine

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-664-16
Digits Only 6332366416
Product NDC 63323-664
Description

25 VIAL in 1 TRAY (63323-664-16) / 1 mL in 1 VIAL (63323-664-41)

Marketing

Marketing Status
Marketed Since 2002-08-01
Brand diphenhydramine
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": "38e8f892-3aa1-473f-9906-8b7ee5d23e89", "openfda": {"upc": ["0363323664411"], "unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["921b9f64-1096-46db-866a-67f0f9ff6790"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (63323-664-16)  / 1 mL in 1 VIAL (63323-664-41)", "package_ndc": "63323-664-16", "marketing_start_date": "20020801"}], "brand_name": "Diphenhydramine", "product_id": "63323-664_38e8f892-3aa1-473f-9906-8b7ee5d23e89", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63323-664", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diphenhydramine", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA040466", "marketing_category": "ANDA", "marketing_start_date": "20020801", "listing_expiration_date": "20261231"}