NDC directory

Zongertinib

Zongertinib · AGC Pharma Chemicals Europe, S.L.U. · POWDER

65404-011BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDINGBulk ingredient
Product NDC
65404-011
Generic name
Zongertinib
Labeler name
AGC Pharma Chemicals Europe, S.L.U.
Finished
false
Listing expiration date
20271231
Marketing category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Dosage form
POWDER
SPL ID
5b912966-134d-6612-e063-6394a90aae00
Product type
BULK INGREDIENT
Marketing start date
20261001
Product ID
65404-011_5b912966-134d-6612-e063-6394a90aae00
Active ingredients
  1. Name
    ZONGERTINIB
    Strength
    1 kg/kg
Packaging
  1. Package NDC
    65404-011-99
    Description
    1 BAG in 1 DRUM (65404-011-99) / 1 BAG in 1 BAG (65404-011-02) / 20 kg in 1 BAG (65404-011-01)
    Marketing start date
    01-OCT-26
Wholesale access for licensed clinicians.

Free to join: your NPI is checked against the federal registry at signup, then wholesale pricing and the professional shelves open.

Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.