Package 51754-0500-1

Brand: caffeine citrate

Generic: caffeine citrate
NDC Package

Package Facts

Identity

Package NDC 51754-0500-1
Digits Only 5175405001
Product NDC 51754-0500
Description

1 VIAL in 1 CARTON (51754-0500-1) / 3 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2015-03-30
Brand caffeine citrate
Generic caffeine citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0408e50a-e029-40d6-9ccf-2399edbcddf9", "openfda": {"unii": ["U26EO4675Q"], "rxcui": ["849931"], "spl_set_id": ["f423a220-e7bf-4d24-bc52-bafc1864265b"], "manufacturer_name": ["Exela Pharma Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (51754-0500-1)  / 3 mL in 1 VIAL", "package_ndc": "51754-0500-1", "marketing_start_date": "20150330"}], "brand_name": "caffeine citrate", "product_id": "51754-0500_0408e50a-e029-40d6-9ccf-2399edbcddf9", "dosage_form": "INJECTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "51754-0500", "generic_name": "caffeine citrate", "labeler_name": "Exela Pharma Sciences, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "caffeine citrate", "active_ingredients": [{"name": "CAFFEINE CITRATE", "strength": "20 mg/mL"}], "application_number": "ANDA077233", "marketing_category": "ANDA", "marketing_start_date": "20150330", "listing_expiration_date": "20261231"}