Home NDC 85380-1001 DECONIMO Reconstitution
Product NDC 85380-1001
11-digit product format 853801001
Labeler code 85380
Product ID 85380-1001_57ab9b1c-9a19-3786-e063-6394a90a2c63
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name DECONIMO Reconstitution
Dosage form SOLUTION
Route INTRAVENOUS
Labeler Image Amazon LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-07-01
Substance WATER
Active strength 1000 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base DECONIMO Reconstitution
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WATER 1000 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 059QF0KO0R Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85380-1001-1 85380100101 30 mL in 1 VIAL (85380-1001-1) 30 ml 2026-07-01 No No Current