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Decitabine Injection shortage

Decitabine Injection is currently listed in shortage by the FDA. The FDA lists 2 affected products. This page was last refreshed from FDA data on Oct 5, 2026.

To Be Discontinued ⚠ Supply risk: High Oncology 2 products 227 days First posted Feb 20, 2026 Updated Feb 20, 2026
Here’s the bottom line

BluePoint Laboratories is permanently stopping its decitabine injection 50 mg. Other makers — including Hikma, Accord Healthcare, Sagent, and Camber — still list this medicine as available.

Don’t stop or change your therapy on your own — talk with your prescriber about the plan that fits you, and ask your pharmacist what’s actually available (see options).

Do you take this drug? See the ‘What to do’ recommendation from Dr. Brian Staiger, PharmD →
2
Affected NDCs
1
Reporting manufacturers
0/1
Reporting mfrs supplying
0/1
Affected strengths supplied
227
Days in shortage
18
Medicaid Rx (2025)
Source: FDA Drug Shortages Database API (openFDA). Last refreshed Oct 5, 2026 · today

What’s in shortage — at a glance

These figures count only the manufacturers that reported this shortage to the FDA — not every company that makes Decitabine Injection. Other makers that haven’t reported a problem are shown in the green card below.

Availability of affected NDCs
From the FDA shortage report
2 NDCs
To be discontinued 2
Affected strengths still supplied
Among manufacturers reporting this shortage
0/1 strengths
No supply 1
FDA-reporting manufacturers with supply
Among manufacturers reporting this shortage
0/1 makers
No supply 1
✓ Other manufacturers not reporting a shortage
Still-marketed Decitabine Injection from companies that have not filed an FDA shortage — these are not counted in the figures above. Stock can still vary by pharmacy.
Hikma Pharmaceuticals USA Inc. Accord Healthcare Inc. Sagent Pharmaceuticals Camber Pharmaceuticals, Inc. Dr. Reddy's Laboratories Inc. Dr.Reddy's Laboratories Limited Eugia US LLC Mylan Institutional LLC BluePoint Laboratories Amneal Pharmaceuticals LLC Meitheal Pharmaceuticals Inc.
Plus 1 alternative dosage form of Decitabine.
See all other options & details →
Shortage timeline
  1. Feb 20, 2026
    Currently in shortage
    2 of 2 products affected.
  2. Feb 20, 2026
    First reported to the FDA
    2 products first listed.

Built from FDA posting and update dates. The end date FDA publishes is the posting/update date, not a true resolution date, so durations are approximate.

What exactly is on backorder — by manufacturer

Manufacturer: Ingenus Pharmaceuticals LLC 📞 866-321-5031 2 NDCS click to expand
Status NDC / product Strength Availability Related information Reason
To Be Discontinued Decitabine, Injection, 50 mg (NDC 50742-430-01) NDC 50742-0430-01 — — Discontinuation of the manufacture of the drug —
To Be Discontinued Decitabine, Injection, 50 mg (NDC 68001-573-41) NDC 68001-0573-41 — — Labeler: BluePoint Laboratories; Discontinuation of the manufacture of the drug —

These rows are manufacturer reports to the FDA for Decitabine Injection — they do not necessarily cover every manufacturer that makes this drug. A company appears here only if it told the FDA it has a supply problem, so other makers may still have stock. That’s the basis for the Where else can I get Decitabine Injection? options further down this page.

Why is Decitabine Injection in shortage?

From what's been reported to the FDA, Ingenus Pharmaceuticals (which also markets this product under the BluePoint Laboratories label) is permanently stopping the manufacture of their 50 mg Decitabine Injection. This applies to both versions of the 50 mg product they make. No specific reason was shared publicly for why they made this decision — just that production is being discontinued.

It's worth knowing that this report only reflects what Ingenus/BluePoint has filed with the FDA. It speaks only to their 50 mg product being permanently pulled from production — not to every maker of decitabine out there.

Based on the manufacturer-reported reason(s) and notes on file with the FDA for Decitabine Injection, summarized in plain English by HelloPharmacist. A drug can be short for more than one reason, and the FDA updates these as manufacturers report changes.

What should I do if I take Decitabine Injection?

Decitabine Injection is currently on the FDA shortage list. This note is to help you understand what that means and what steps make sense next.

The affected strength is the 50 mg injection. Right now, the manufacturer on this record (listed under BluePoint Laboratories) reports no available supply of this 50 mg product. The status is listed as "to be discontinued," which means this particular supply problem may be permanent rather than a short-term gap.

Because this is a discontinuation rather than a temporary delay, the most important thing is to plan ahead with your care team. Keep in mind this report reflects only the manufacturer(s) that filed it. Several other companies make the same medicine — decitabine 50 mg injection — so it may still be obtainable from another source.

Here is what I suggest, in order:

  1. Do not stop or change your treatment on your own — this medicine is used under close medical supervision, so any change should come from your care team.
  2. Ask your pharmacy to check whether the same medicine is available from another maker, such as Hikma, Accord, Sagent, Camber, Dr. Reddy's, Eugia, Mylan, Amneal, or Meitheal; it may not be in local stock.
  3. If it cannot be found, talk with your prescriber about a clinician-chosen option.

Manufacturer contact numbers are listed on this page for reference, though pharmacies usually handle those calls. This is general, national information and may not match your local pharmacy's actual stock.

See “Where else can I get Decitabine Injection?” below ↓ The same medicine from manufacturers not reporting a shortage, alternative dosage forms, and therapeutic equivalents with pricing.
If you are a patient:
  • Don’t stop or change the medication on your own — talk to your prescriber first.
  • If this is part of an ongoing or essential regimen (for example HIV treatment or prevention, seizure, heart, transplant, diabetes or mental-health medicines), do not skip or ration doses — contact your pharmacist or prescriber right away to arrange continued supply before you run out.
  • Ask your pharmacy to check other manufacturers, strengths, package sizes, and nearby stores.
  • Ask your prescriber whether a different strength, formulation, or the brand/generic version is appropriate.
Keep reading
Our full Decitabine Injection guide

Uses, dosing, side effects, prices, and the complete FDA label — written in plain English and pharmacist-reviewed.

Read the Decitabine Injection guide →

Where else can I get Decitabine Injection?

FDA shortages are manufacturer-reported — a company only shows up on the shortage list if it told the FDA it has a supply problem, so not every maker of Decitabine Injection is necessarily short. Below we pull together the other still-marketed options that are not reported in shortage: the same medicine from manufacturers that haven’t reported a problem, and alternative dosage forms. These may still be out of stock at your pharmacy, and only your prescriber or pharmacist can decide what’s right for you.

Same medicine, other manufacturers (not reported short)

Same active ingredient, dosage form & route as the shortage (matched on the FDB HICL ingredient code), from makers that have not filed a shortage with the FDA:

ProductStrengthForm / routeManufacturerNDC
Decitabine DECITABINE 50 mg/1 Injection, Powder, Lyophilized, For Solution · Intravenous Hikma Pharmaceuticals USA Inc. 00143-9385-01
Decitabine DECITABINE 50 mg/20mL Injection, Powder, Lyophilized, For Solution · Intravenous Accord Healthcare Inc. 16729-0224-05
Decitabine DECITABINE 50 mg/20mL Injection, Powder, Lyophilized, For Solution · Intravenous Sagent Pharmaceuticals 25021-0219-20
Decitabine DECITABINE 50 mg/10mL Injection, Powder, Lyophilized, For Solution · Intravenous Camber Pharmaceuticals, Inc. 31722-0304-31
Decitabine DECITABINE 50 mg/10mL Injection, Powder, Lyophilized, For Solution · Intravenous Dr. Reddy's Laboratories Inc. 43598-0427-37
Decitabine DECITABINE 50 mg/10mL Injection, Powder, Lyophilized, For Solution · Intravenous Dr.Reddy's Laboratories Limited 55111-0556-10
Decitabine DECITABINE 50 mg/26mL Injection, Powder, Lyophilized, For Solution · Intravenous Eugia US LLC 55150-0376-01
Decitabine DECITABINE 50 mg/20mL Injection, Powder, Lyophilized, For Solution · Intravenous Mylan Institutional LLC 67457-0316-25
Decitabine DECITABINE 50 mg/20mL Injection, Powder, Lyophilized, For Solution · Intravenous BluePoint Laboratories 68001-0618-37
Decitabine DECITABINE 50 mg/10mL Injection, Powder, Lyophilized, For Solution · Intravenous BluePoint Laboratories 68001-0642-41
Decitabine DECITABINE 50 mg/20mL Injection, Powder, Lyophilized, For Solution · Intravenous Amneal Pharmaceuticals LLC 70121-1644-01
Decitabine DECITABINE 50 mg/20mL Injection, Powder, Lyophilized, For Solution · Intravenous Meitheal Pharmaceuticals Inc. 71288-0119-20

Alternative dosage forms of Decitabine

A different form of the same drug (for example a solution when capsules are short). A form change is a clinical decision — ask your prescriber:

Therapeutic equivalents & pricing 22 productsclick to expand

Orange Book–rated equivalents of the affected strengths, with the latest NADAC price (a federal retail-acquisition benchmark, not your copay) and an evidence-based availability label. Cheapest first.

ProductManufacturerPackageNADAC $/unitAB ratingAvailability
decitabine 50 mgNDC 00143-9385-01 Hikma 1 vial — AP FDA listed
Decitabine 50 mg/20mLNDC 16729-0224-05 Accord 1 vial — AP FDA listed
Decitabine 50 mg/20mLNDC 25021-0219-20 Sagent 1 vial — AP FDA listed
Decitabine 50 mg/10mLNDC 31722-0304-31 Camber 1 vial — AP FDA listed
Decitabine 50 mg/10mLNDC 43598-0427-37 Dr. 1 vial — AP FDA listed
decitabineNDC 47335-0361-41 Sun 1 kit — — FDA listed
Decitabine 50 mg/10mLNDC 55111-0556-10 Dr.Reddy's 1 vial — AP FDA listed
Decitabine 50 mg/26mLNDC 55150-0376-01 Eugia 1 vial — — FDA listed
Decitabine 50 mg/20mLNDC 67184-0535-01 Qilu 1 vial — AP FDA listed
Decitabine 50 mg/20mLNDC 67457-0316-25 Mylan 1 vial — AP FDA listed
Decitabine 50 mgNDC 68001-0573-41 BluePoint 1 vial — — FDA listed
Decitabine 50 mg/20mLNDC 68001-0618-37 BluePoint 1 vial — AP FDA listed
Decitabine 50 mg/10mLNDC 68001-0642-41 BluePoint 1 vial — AP FDA listed
decitabine 50 mg/10mLNDC 68083-0528-01 Gland 1 vial — AP FDA listed
Decitabine 50 mg/20mLNDC 70121-1644-01 Amneal 1 vial — AP FDA listed
Decitabine 50 mg/20mLNDC 71288-0119-20 Meitheal 1 vial — AP FDA listed
Decitabine 50 mg/10mLNDC 72162-2634-02 Bryant 1 vial — AP FDA listed
Decitabine 50 mg/10mLNDC 72205-0031-01 Novadoz 1 vial — AP FDA listed
Decitabine 50 mg/10mLNDC 72205-0036-01 Novadoz 1 vial — AP FDA listed
Decitabine 50 mg/10mLNDC 72603-0107-01 Northstar 1 vial — AP FDA listed
Decitabine 50 mg/20mLNDC 75834-0190-01 Nivagen 1 vial — AP FDA listed
Decitabine 50 mgNDC 50742-0430-01 Ingenus 1 vial — — Discontinued

Equivalents share the same ingredient, strength, dosage form and route; an AB rating means the FDA considers them substitutable. NADAC is a national retail-pharmacy acquisition benchmark from CMS — not what you pay. Availability is inferred from recent pricing, not a stock check.

Other drugs in the same treatment class

These are different medicines — not other versions of Decitabine Injection — that fall in the same broad treatment class (antineoplastic - antimetabolites) . They are not automatic substitutes: they can differ in how they work, dosing, effectiveness, side effects and what they’re approved to treat. Do not switch on your own. This list is for information only — ask your prescriber or pharmacist whether any of them is appropriate for you.

Identity & classification

GCN Seq No 060839
GCN 27027
HICL code 033712
Ingredient (HICL) Decitabine
HIC1 code V
Therapeutic class — broad (HIC1) Neoplasms
HIC2 code V1
Therapeutic class — intermediate (HIC2) Antineoplastic Drugs
HIC3 code V1B
Therapeutic class — specific (HIC3) Antineoplastic - Antimetabolites
AHFS code 10:00.00.00
AHFS class Antineoplastic Agents
FDB label name DECITABINE 50 MG VIAL
FDB brand name Decitabine
Legend status F — Federal legend — prescription drug or device
Where does this data come from?
Identity codes come from First Databank (FDB) (HICL ingredient, HIC1–3 therapeutic-class hierarchy, GCN, AHFS class, legend status) and Medi-Span GPI, mapped from a representative affected NDC. Licensed reference data — for identification only.

Other oncology shortages

Decitabine Injection shortage FAQs

Is Decitabine Injection in shortage?
Yes — the FDA currently lists Decitabine Injection in shortage (status: “To Be Discontinued”, first reported Feb 20, 2026). 2 of 2 products are affected. This is national, manufacturer-reported data, so your pharmacy may still have stock.
Which products are affected?
Decitabine, Injection, 50 mg (NDC 50742-430-01) (NDC 50742-0430-01); Decitabine, Injection, 50 mg (NDC 68001-573-41) (NDC 68001-0573-41). The full per-NDC list (availability, manufacturer and status) is in the table above — each NDC links to its own page.
When will Decitabine Injection be available again?
The FDA does not publish a guaranteed restock date, and no estimated-recovery note is on file. Availability can change daily — confirm with your pharmacy.
Can I still get Decitabine somewhere?
Other manufacturers (Hikma Pharmaceuticals USA Inc., Accord Healthcare Inc., Sagent Pharmaceuticals and others) still market it and have not reported a shortage. 1 alternative dosage form of Decitabine is also listed. See “Where else can I get Decitabine Injection?” above — stock still varies by pharmacy.
What should I do if I take Decitabine Injection?
Don’t stop or change it on your own. Ask your pharmacist whether they can order it from another manufacturer or a different strength/package size, and ask your prescriber about a long-term plan before your supply runs out.

Still have a question about the Decitabine Injection shortage?

Ask a pharmacist about this shortage →
How to read the Supply-Risk rating
Low (1–2)Multiple manufacturers still supplying and most strengths or pack sizes sourceable.
Medium (3)Some constraint — fewer suppliers or a notable share of NDCs unavailable.
High (4–5)Down to a single source, most strengths or pack sizes unsourceable, or a long-running outage.
Where does this data come from?
Shortage records come from the FDA Drug Shortages Database API via openFDA (/drug/shortages) — drug, manufacturer & contact, NDC/product, status, availability, reason, therapeutic category and posting/update dates. Current / To Be Discontinued = active; Resolved is kept for history. The Supply-Risk rating is assessed per active ingredient and adds the FDA NDC Directory (still-marketed manufacturers by ingredient & form); same-medicine and equivalent products use First Databank classification + CMS NADAC pricing; Medicaid use + most-affected states come from CMS Medicaid State Drug Utilization Data. Reference only — confirm current status with the manufacturer or FDA before acting on it.
Data structure & sourcing designed and verified by Dr. Brian Staiger, PharmD.
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