United States · FDA National Drug Code directory
Renflexis
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 78206-162_20c46bec-ae83-4851-98b7-88222a8ff88a
- Product NDC
- 78206-162
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- infliximab
- Labeler
- Organon LLC
- Marketing category
- BLA
- Marketing start / end (source format)
- 20170421
- Source listing expiry
- 20271231
Source-listed ingredients
- INFLIXIMAB — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (78206-162-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (78206-162-99) · 78206-162-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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