Azacitidine 100 mg injection, powder, lyophilized, for solution

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Armas Pharmaceuticals Inc. names for other drugs.

Recalls

• Dec 8, 2020 · Class II · Shilpa Medicare Limited
  CGMP Deviations
  Lots: Lot #s: 7S10115A, Exp. 07/31/2021; 7S10143A, 7S10182B, Exp. 09/30/2021; 7S10255A, 7S10256A, 7S10263A, Exp. 11/30/2021; 7T10028A, 12/31/2021; 7T10040A, Exp. 01/31/2022.

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Azacitidine: every company that makes it

Form

injection, powder, lyophilized, for solution, intravenous; subcutaneous

Strength

100 mg

Approval

ANDA ANDA207518

On the market since

Sep 10, 2018

Package NDCs

72485-201-01

Official label

DailyMed (National Library of Medicine), updated Aug 5, 2025

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?