United States · FDA National Drug Code directory

MYXREDLIN

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
0338-0126_9642c441-5143-410a-af83-db5daded5420
Product NDC
0338-0126
Form
INJECTION, SOLUTION
Composition / generic term
insulin human
Labeler
Baxter Healthcare Corporation
Marketing category
BLA
Marketing start / end (source format)
20190712
Source listing expiry
20271231

Source-listed ingredients

  • INSULIN HUMAN — 1 [iU]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 12 CONTAINER in 1 CARTON (0338-0126-12) / 100 mL in 1 CONTAINER · 0338-0126-12

Source and coverage

Open FDA National Drug Code directory

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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