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
SOLUTION
Routes
Active Ingredients
caffeine citrate 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-406
Product ID
63323-406_8d47943c-b6f3-4742-90fe-4667e19c8605
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078002
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
63323406
Hyphenated Format
63323-406
Supplemental Identifiers
RxCUI
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
ANDA078002 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 5 VIAL in 1 CARTON (63323-406-03) / 3 mL in 1 VIAL (63323-406-01)
Packages (1)
Ingredients (1)
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"}