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testosterone cypionate 200 mg/mL Injection, Solution — NDC 82983-0424-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

testosterone cypionate 200 mg/mL Injection, Solution — NDC 82983-424-01 (Billing 82983-0424-01)

by Ajenat Pharmaceuticals LLC · 1 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE

This is a package of testosterone cypionate 200 mg/mL Injection, Solution from Ajenat Pharmaceuticals LLC, marketed since Sep 2026 and currently FDA-listed. It is this product's only package size.

NDC 82983-0424-01
🏷️ FDA NDC (as labeled) 82983-424-01 billing pads the product segment with a zero
Rx only Generic On market CIII ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 82983-424-01 alone.

Record
FDA NDC Directory package listing · Human prescription drug
Code segments
82983 labeler · 424 product · 01 package
Package marketed since
Sep 14, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8298342401 2
FDA record last changed
Oct 8, 2026
⚠️
Other active recalls for Testosterone Cypionate (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 10, 2025 — cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials. (Eugia US LLC) · FDA recall D-0363-2025
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 82983-424-01
Product NDC 82983-424
11-digit billing NDC 82983042401
Application # ANDA219478
SPL Set ID cd57648c-ce53-459a-9f14-3984fc464428
Established class (EPC) Androgen
Mechanism of action Androgen Receptor Agonists
Chemical class Androstanes
DEA schedule CIII
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-09-14
Route INTRAMUSCULAR
Dosage form INJECTION, SOLUTION
Substance TESTOSTERONE CYPIONATE
TE code (Orange Book) AO · RLD · RS
Why two NDCs? The FDA registers this code as 82983-424-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 82983-0424-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It's for adult men whose bodies make too little testosterone, called hypogonadism. Your doctor should confirm this with morning blood tests on at least two different days before st...
  • Testosterone gel can pass to others through skin contact. Children and women should avoid touching unwashed or unclothed application sites, and you should follow the instructions f...
  • How do I keep my family safe if I use a gel?
  • Common ones include a higher PSA, mood changes, acne, higher blood pressure and skin irritation. Your doctor will check blood tests such as PSA and blood counts and monitor your bl...
📖 Read our full Testosterone guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
82983-0424-01 You're viewing this Main listing 1 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE 2026-09-14 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
testosterone cypionate 200 mg/mL 47781-0910-91 Alvogen 10 vials $2.311 AO Availability likely —
Testosterone Cypionate 200 mg/mL 62756-0016-40 Sun 1 vial $3.286 — FDA listed —
Testosterone Cypionate 200 mg/mL 00143-9726-01 Hikma 10 ml $3.582 AO Availability likely —
Testosterone Cypionate 200 mg/mL 00143-9005-01 Hikma 1 vial $3.582 AO Availability likely —
testosterone cypionate 200 mg/mL 70700-0290-22 Xiromed 1 vial $3.582 AO Availability likely —
Testosterone Cypionate 200 mg/mL 62756-0015-40 Sun 1 vial $11.349 — FDA listed —
Testosterone Cypionate 200 mg/mL 00574-0827-01 Padagis 1 vial $11.392 AO Availability likely —
Testosterone Cypionate 200 mg/mL 00143-9659-01 Hikma 1 ml $11.392 AO Availability likely —
Testosterone Cypionate 200 mg/mL 69097-0802-32 Cipla 1 vial $11.392 AO Availability likely —
Testosterone Cypionate 200 mg/mL 00409-6562-01 Hospira, 1 vial $11.392 AO Availability likely —
Testosterone Cypionate 200 mg/mL 55150-0277-01 Eugia 1 vial $11.392 AO Availability likely —
testosterone cypionate 200 mg/mL 72603-0286-01 NorthStar 1 vial $11.392 AO Availability likely —
Testosterone Cypionate 200 mg/mL 69097-0537-31 Cipla 1 ml $11.392 AO Availability likely —
Testosterone Cypionate 200 mg/mL 00574-0820-01 Padagis 1 vial $11.392 AO Availability likely —
testosterone cypionate 200 mg/mL 47781-0911-93 Alvogen 1 vial $11.392 AO Availability likely —
Testosterone Cypionate 200 mg/mL 52536-0625-01 Wilshire 1 vial $11.392 AO Availability likely —
testosterone cypionate 200 mg/mL 70700-0289-22 Xiromed 1 vial $11.392 AO Availability likely —
Depo-Testosterone 200 mg/mL 00009-0086-01 Pharmacia 1 vial $14.140 AO Availability likely —
Depo-Testosterone 200 mg/mL 00009-0417-01 Pharmacia 1 vial $14.140 AO Availability likely —
Testosterone Cypionate 200 mg/mL 00517-1830-01 American 1 vial $14.181 AO Discontinued —
Testosterone Cypionate 200 mg/mL 63187-0647-10 Proficient 10 ml — AO FDA listed —
Testosterone Cypionate 200 mg/mL 71205-0289-01 Proficient 1 ml — AO FDA listed —
Testosterone Cypionate 200 mg/mL 76420-0065-10 Asclemed 10 ml — AO FDA listed —
Testosterone Cypionate 200 mg/mL 63629-8706-01 Bryant 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 76420-0645-10 Asclemed 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 76420-0741-10 Asclemed 1 vial — AO FDA listed —
testosterone cypionate 200 mg/mL 76420-0747-01 Asclemed 1 vial — AO FDA listed —
Azmiro 200 mg/mL 24338-0055-01 Azurity 1 syringe — — FDA listed —
Azmiro 200 mg/mL 24338-0056-01 Azurity 1 vial — — FDA listed —
testosterone cypionate 200 mg/mL 68071-3840-01 NuCare 10 vials — AO FDA listed —
Testosterone Cypionate 200 mg/mL 50090-4147-00 A-S 1 vial — AO FDA listed —
testosterone cypionate 200 mg/mL 50090-7585-00 A-S 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 50090-7435-00 A-S 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 71335-2470-01 Bryant 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 72162-2348-02 Bryant 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 68071-3809-01 NuCare 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 72162-1119-02 Bryant 1 vial — AO FDA listed —
testosterone cypionate 200 mg/mL 68071-3835-01 NuCare 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 50090-4920-00 A-S 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 63629-8705-01 Bryant 1 vial — AO FDA listed —
testosterone cypionate 200 mg/mL 76420-0752-10 Asclemed 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 70518-4538-00 REMEDYREPACK 1 ml — AO FDA listed —
Testosterone Cypionate 200 mg/mL 71335-2473-01 Bryant 1 vial — AO FDA listed —
testosterone cypionate 200 mg/mL 50090-7584-00 A-S 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 76420-0746-01 Asclemed 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 71335-2838-01 Bryant 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 72162-2375-02 Bryant 1 vial — AO FDA listed —
Testosterone Cypionate 200 mg/mL 87063-0272-10 ASCLEMED 1 vial — AO FDA listed —
testosterone cypionate 200 mg/mL 82983-0425-01 Ajenat 1 vial — AO FDA listed —
testosterone cypionate 200 mg/mLthis 82983-0424-01 Ajenat 1 vial — AO FDA listed —
testosterone cypionate 200 mg/mL 54288-0150-01 BPI 1 vial — AO FDA listed —
testosterone cypionate 200 mg/mL 54288-0156-01 BPI 1 vial — AO FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2026
On the market since
Sep 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

🧪 Avoiding an ingredient? See Testosterone inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • 9.45 mg / 1 mL UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • 0.2 mL / 1 mL UNII N863NB338G
    Benzyl benzoate is a liquid organic compound used as a solvent and preservative in medicines. It helps dissolve active ingredients and can extend shelf life by preventing microbial growth in liquid formulations.
  • 560 mg / 1 mL UNII H3E878020N
    Cottonseed oil is a natural vegetable oil extracted from cotton plant seeds. It is used in medicines as a solvent and lubricant to help dissolve active ingredients and allow smooth tablet or capsule movement through manufacturing equipment.

3 inactive ingredients listed in the exact product block matched to this NDC.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerAjenat Pharmaceuticals LLC
Application holderBPI LABS LLC
FDA applicationANDA219478 (ANDA)
Labeler code82983
First marketedSep 2026
DEA scheduleCIII
Product typeHuman Prescription Drug
Portfolio15 products on file

More NDCs from Ajenat Pharmaceuticals LLC labeler code 82983

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label
📄 FDA label 19 words ▾

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Testosterone Cypionate — the program that covers self-administered drugs. 12 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Testosterone Cypionate. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$11.24M
Claims incl. refills
320.7K
Beneficiaries
209.5K
Spend / beneficiary
$53.62
Spend / claim
$35.03
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

About this NDC listing & data coverage

Finished prescription product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data ✓ Available
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Ajenat Pharmaceuticals LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Ajenat Pharmaceuticals LLC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 82983-0423-47 · Ajenat 82983-0425-01 · Ajenat →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.