caffeine citrate
Generic: caffeine citrate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
caffeine citrate
Generic Name
caffeine citrate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
caffeine citrate 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-407
Product ID
63323-407_2c3a55e5-1b61-4ed2-adca-c3beb44baf14
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077997
Listing Expiration
2026-12-31
Marketing Start
2009-11-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323407
Hyphenated Format
63323-407
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
caffeine citrate (source: ndc)
Generic Name
caffeine citrate (source: ndc)
Application Number
ANDA077997 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1 VIAL in 1 BOX (63323-407-03) / 3 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2c3a55e5-1b61-4ed2-adca-c3beb44baf14", "openfda": {"upc": ["0363323407032"], "unii": ["U26EO4675Q"], "rxcui": ["849931"], "spl_set_id": ["baf9f88a-776a-44e7-82cc-8f0ca419572f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (63323-407-03) / 3 mL in 1 VIAL", "package_ndc": "63323-407-03", "marketing_start_date": "20091119"}], "brand_name": "Caffeine Citrate", "product_id": "63323-407_2c3a55e5-1b61-4ed2-adca-c3beb44baf14", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "63323-407", "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": "ANDA077997", "marketing_category": "ANDA", "marketing_start_date": "20091119", "listing_expiration_date": "20261231"}