United States · FDA National Drug Code directory

Penpulimab kcqx

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
83654-105_5af2c808-a2ec-623f-e063-6294a90a6d99
Product NDC
83654-105
Form
INJECTION
Composition / generic term
Penpulimab
Labeler
Akeso Biopharma, Co., Ltd
Marketing category
BLA
Marketing start / end (source format)
20250423
Source listing expiry
20271231

Source-listed ingredients

  • PENPULIMAB — 100 mg/10mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-DOSE in 1 BOX (83654-105-01) / 10 mL in 1 VIAL, SINGLE-DOSE · 83654-105-01

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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Penpulimab kcqx — United States | Molindra Medicines