Package 42571-169-55

Brand: diphenhydramine

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42571-169-55
Digits Only 4257116955
Product NDC 42571-169
Description

10 AMPULE in 1 CARTON (42571-169-55) / 1 mL in 1 AMPULE (42571-169-54)

Marketing

Marketing Status
Marketed Since 2018-12-04
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": "4c46492b-00c4-8ee4-e063-6294a90a6914", "openfda": {"upc": ["0342571337957", "0342571169541"], "unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["a1110433-498a-48cb-ac79-5732fd4f8fba"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (42571-169-55)  / 1 mL in 1 AMPULE (42571-169-54)", "package_ndc": "42571-169-55", "marketing_start_date": "20181204"}], "brand_name": "DIPHENHYDRAMINE", "product_id": "42571-169_4c46492b-00c4-8ee4-e063-6294a90a6914", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "42571-169", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIPHENHYDRAMINE", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA205723", "marketing_category": "ANDA", "marketing_start_date": "20181204", "listing_expiration_date": "20271231"}