United States · FDA National Drug Code directory

Adalimumab

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
61314-332_ae54abc4-e9c5-4c5a-8fa7-968e5ad72050
Product NDC
61314-332
Form
INJECTION, SOLUTION
Composition / generic term
adalimumab-adaz
Labeler
Sandoz Inc
Marketing category
BLA
Marketing start / end (source format)
20241202
Source listing expiry
20271231

Source-listed ingredients

  • ADALIMUMAB — 20 mg/.2mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 SYRINGE, GLASS in 1 CARTON (61314-332-64) / .2 mL in 1 SYRINGE, GLASS · 61314-332-64

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.

Browse United States records →