Package 63323-406-03

Brand: caffeine citrate

Generic: caffeine citrate
NDC Package

Package Facts

Identity

Package NDC 63323-406-03
Digits Only 6332340603
Product NDC 63323-406
Description

5 VIAL in 1 CARTON (63323-406-03) / 3 mL in 1 VIAL (63323-406-01)

Marketing

Marketing Status
Marketed Since 2009-11-19
Brand caffeine citrate
Generic caffeine citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8d47943c-b6f3-4742-90fe-4667e19c8605", "openfda": {"unii": ["U26EO4675Q"], "rxcui": ["849928"], "spl_set_id": ["b4fb7c77-1e82-48b7-83c5-dd04ec7c5c4e"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (63323-406-03)  / 3 mL in 1 VIAL (63323-406-01)", "package_ndc": "63323-406-03", "marketing_start_date": "20091119"}], "brand_name": "Caffeine Citrate", "product_id": "63323-406_8d47943c-b6f3-4742-90fe-4667e19c8605", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "63323-406", "generic_name": "CAFFEINE CITRATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Caffeine Citrate", "active_ingredients": [{"name": "CAFFEINE CITRATE", "strength": "20 mg/mL"}], "application_number": "ANDA078002", "marketing_category": "ANDA", "marketing_start_date": "20091119", "listing_expiration_date": "20261231"}