caffeine citrate
Generic: caffeine citrate
Labeler: exela pharma sciences, llcDrug Facts
Product Profile
Brand Name
caffeine citrate
Generic Name
caffeine citrate
Labeler
exela pharma sciences, llc
Dosage Form
INJECTION
Routes
Active Ingredients
caffeine citrate 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51754-0500
Product ID
51754-0500_0408e50a-e029-40d6-9ccf-2399edbcddf9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077233
Listing Expiration
2026-12-31
Marketing Start
2015-03-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
517540500
Hyphenated Format
51754-0500
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
ANDA077233 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1 VIAL in 1 CARTON (51754-0500-1) / 3 mL in 1 VIAL
Packages (1)
Ingredients (1)
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"}