NDC 62756-290 - CAFFEINE CITRATE

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 62756-290
Package NDCs from labels: 62756-290-40, 62756-290-44
Manufacturer: Sun Pharmaceutical Industries Ltd
Effective date: 2009-10-02
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
CAFFEINE CITRATE - Sun Pharmaceutical Industries Ltd	Sun Pharmaceutical Industries Ltd	2009-10-02	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62756-290	CAFFEINE CITRATE INJECTION CAFFEINE CITRATE SOLUTION [SUN PHARMACEUTICAL INDUSTRIES LTD]	1	Unmatched	20091009_dfa7e0a9-eac0-4741-9b85-69c122f13e33.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAFFEINE CITRATE	ACTIVE INGREDIENT	U26EO4675Q	CAFFEINE CITRATE INJECTION CAFFEINE CITRATE SOLUTION [SUN PHARMACEUTICAL INDUSTRIES LTD]	1
CAFFEINE	ACTIVE MOIETY	3G6A5W338E	CAFFEINE CITRATE INJECTION CAFFEINE CITRATE SOLUTION [SUN PHARMACEUTICAL INDUSTRIES LTD]	1
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	CAFFEINE CITRATE INJECTION CAFFEINE CITRATE SOLUTION [SUN PHARMACEUTICAL INDUSTRIES LTD]	1
TRISODIUM CITRATE DIHYDRATE	INACTIVE INGREDIENT	B22547B95K	CAFFEINE CITRATE INJECTION CAFFEINE CITRATE SOLUTION [SUN PHARMACEUTICAL INDUSTRIES LTD]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	CAFFEINE CITRATE INJECTION CAFFEINE CITRATE SOLUTION [SUN PHARMACEUTICAL INDUSTRIES LTD]	1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 14 of 14 · 261 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
159b5dcd-d7c4-4504-8a48-a9a8e47e9656			dfa7e0a9-eac0-4741-9b85-69c122f13e33	2009-10-02	Warnings, Adverse reactions	Exact identifier spl id: 159b5dcd-d7c4-4504-8a48-a9a8e47e9656 spl set id: dfa7e0a9-eac0-4741-9b85-69c122f13e33

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.