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Flecainide Acetate 50 mg Tablet, 100-count — NDC 65862-621-01 (Billing 65862-0621-01)

by Aurobindo Pharma Limited · 100 TABLET in 1 BOTTLE

This is a package of 100 tablets of Flecainide Acetate 50 mg Tablet from Aurobindo Pharma Limited, marketed since Jul 2015 and currently FDA-listed; retail pharmacies pay about $0.1084 per tablet (NADAC). It is the main listing for this product, which comes in 4 package sizes.

NDC 65862-0621-01
🏷️ FDA NDC (as labeled) 65862-621-01 billing pads the product segment with a zero
This package
Contains100-count Cost per ea$0.1084 NADAC Per package$10.84 / 100 tablets Pack sizes4 compare ↓
Also priced by: Medicaid pays $0.1995/unit · Part D plans $0.2193/unit — full pricing hub ↓
Main listing for product 65862-621 · Also comes in: 30 tablets 65862-621-30 1000 tablets 65862-621-99 12000 tablets 65862-621-53
On market Non-controlled ⇄ 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 65862-621-01 alone.

Record
FDA NDC Directory package listing · Drug for further processing
Code segments
65862 labeler · 621 product · 01 package
Listing certified through
Dec 31, 2026
Billing quantity
100 EA per package
Barcode (UPC-A, from the NDC)
3 6586262101 6
Medicaid fills, this package
2,551 prescriptions in the last four reported quarters
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 65862-621-01
Product NDC 65862-621
11-digit billing NDC 65862062101
NCPDP billing unit EA — each (per item)
SPL Set ID 3650f7e3-c06f-468a-b674-c6f12a531091
DEA schedule Non-controlled
Marketing category DRUG FOR FURTHER PROCESSING
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-07-08
Dosage form TABLET
Substance FLECAINIDE ACETATE

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 35300010100303
GPI class Flecainide Acetate
GCN Seq No 000265
GCN 01581
HICL code 000082
Ingredient (HICL) Flecainide Acetate
HIC1 code A
Therapeutic class — broad (HIC1) Cardiovascular System
HIC2 code A2
Therapeutic class — intermediate (HIC2) Cardiac Depressants
HIC3 code A2A
Therapeutic class — specific (HIC3) Antiarrhythmics
AHFS code 24:04.04.12
AHFS class Class Ic Antiarrhythmics
FDB label name FLECAINIDE ACETATE 50 MG TAB
FDB brand name Flecainide Acetate
Legend status F — Federal legend — prescription drug or device
Quick answers
  • GSN (GCN sequence number): 000265
  • GCN: 01581
  • GPI-14 (Medi-Span): 35300010100303
  • HICL (First Databank): 000082
  • AHFS class code: 24:04.04.12
Why two NDCs? The FDA registers this code as 65862-621-01 — 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 → 65862-0621-01. 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

Label name FLECAINIDE ACETATE 50 MG TAB Ingredient Flecainide Acetate
📖 What it is MedlinePlus · NLM

Flecainide is used to prevent certain types of life-threatening irregular heartbeats. Flecainide is in a class of medications called antiarrhythmics. It works by slowing electrical signals in the heart to stabilize the heart rhythm.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • It helps prevent certain fast heart rhythms, including PSVT and paroxysmal atrial fibrillation/flutter, in people without structural heart disease. It is also used to prevent life-...
  • Take it by mouth exactly as prescribed, usually twice a day. Food and antacids don't change how well it's absorbed. Your doctor will raise the dose slowly, so don't change it on yo...
  • Dizziness and vision changes like blurred vision are the most common. Some people also get shortness of breath, headache, nausea, tiredness, or palpitations. Call your doctor if th...
  • Get emergency help for fainting, a very fast, pounding, or irregular heartbeat, or chest pain. Call your doctor for new swelling, worse shortness of breath, a very slow pulse, yell...
📖 Read our full Flecainide 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 eaPer package
Retail pharmacies payNADAC · weekly $0.108 $10.84 / 100 tablets
Medicaid paysCMS SDUD · 12 mo $0.1995 $19.95 / 100 tablets
Medicare drug plans payPart D · Q2 2026 $0.2193 $21.93 / 100 tablets
NADAC price history (per ea) — tap or hover for the price & month
Jan 2022 Aug 2022 Jan 2026 Sep 2026 $0.156 $0.108
▼ Down 30% over the last 24 months.
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 Per unit Per pack Marketing startMarketing endStatus
65862-0621-01 You're viewing this Main listing 100 TABLET in 1 BOTTLE $0.1084 / ea $10.84 2017-11-03 — Active
65862-0621-30 65862-621-30 30 TABLET in 1 BOTTLE — — 2017-11-03 — Active
65862-0621-99 65862-621-99 1000 TABLET in 1 BOTTLE — — 2017-11-03 — Active
65862-0621-53 65862-621-53 12000 TABLET in 1 BAG — — — — Active

You're viewing one of 4 pack sizes for this product.

In Medicaid, this is the most-dispensed pack of this product — about 100% of fills over the last four reported quarters. See all packs ↓

Pack size FAQ

What quantity is in this package?
This is a 100-count package — 100 tablet in 1 bottle.
How does this package differ from NDC 65862-0621-30?
Both are Flecainide Acetate 50 mg Tablet — the drug itself is identical. This page's package is the 100-count one, while NDC 65862-0621-30 is the 30 tablets package.
What NDC number is used to bill for this package of Flecainide Acetate 50 mg Tablet?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Flecainide Acetate 50 mg 00054-0010-20 Hikma 100 tablets $0.108 AB Availability likely —
Flecainide Acetate 50 mg 42806-0817-01 Epic 100 tablets $0.108 AB Availability likely —
Flecainide Acetate 50 mg 50268-0320-15 AvPAK 50 tablets $0.108 AB Availability likely —
Flecainide Acetate 50 mg 53746-0641-01 Amneal 100 tablets $0.108 AB Availability likely —
Flecainide Acetate 50 mg 57237-0063-01 Rising 100 tablets $0.108 AB Availability likely —
Flecainide Acetate 50 mg 62135-0660-60 Chartwell 60 tablets $0.108 — Availability likely —
Flecainide Acetate 50 mg 62559-0380-01 ANI 100 tablets $0.108 AB Availability likely —
Flecainide Acetate 50 mgthis 65862-0621-01 Aurobindo 100 tablets $0.108 — Availability likely —
Flecainide Acetate 50 mg 76385-0145-01 UNICHEM 100 tablets $0.108 AB Availability likely —
Flecainide Acetate 50 mg 65162-0641-10 Amneal 100 tablets $0.112 AB FDA listed +3%
Flecainide Acetate 50 mg 50090-5306-00 A-S 60 tablets — AB FDA listed —
Flecainide Acetate 50 mg 50090-6035-00 A-S 60 tablets — AB FDA listed —
Flecainide Acetate 50 mg 50090-6810-00 A-S 60 tablets — AB FDA listed —
Flecainide Acetate 50 mg 51407-0018-01 Golden 100 tablets — AB FDA listed —
Flecainide Acetate 50 mg 63629-1946-01 Bryant 100 tablets — AB FDA listed —
Flecainide Acetate 50 mg 63629-7979-01 Bryant 30 tablets — AB Discontinued —
Flecainide Acetate 50 mg 63629-9184-01 Bryant 100 tablets — AB FDA listed —
Flecainide Acetate 50 mg 71335-1487-01 Bryant 30 tablets — AB FDA listed —
Flecainide Acetate 50 mg 71335-2995-01 Bryant 30 tablets — AB FDA listed —
Flecainide Acetate 50 mg 72162-1760-01 Bryant 100 tablets — AB FDA listed —
Flecainide Acetate 50 mg 72789-0385-01 PD-Rx 100 tablets — AB FDA listed —
Flecainide Acetate 50 mg 82804-0155-30 Proficient 30 tablets — AB FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
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

🏛️
2015
On the market since
Jul 2015
📍
2026
Currently FDA-listed
11 years listed
🔓
·
Generic versions listed
see equivalents
✅Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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 Flecainide 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerAurobindo Pharma Limited
Labeler code65862
First marketedJul 2015
Product typeDrug For Further Processing
Portfolio1,464 products on file

More NDCs from Aurobindo Pharma Limited labeler code 65862

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 FDA label FDA SPL

The complete FDA label for this product, 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 ↗

Medicaid utilization & spend

📍 This exact package only: Medicaid data is reported per full 11-digit NDC — labeler, product and pack size — so every number here is for this package alone, not the drug overall. Other pack sizes report separately.
💊 Pharmacy benefit only: These are Medicaid outpatient pharmacy claims, billed by NDC. They exclude the medical benefit — clinic- or hospital-administered drugs billed under HCPCS J-codes — so drugs used mostly that way (e.g. Avastin, Lucentis, Keytruda) can look low or missing here. That’s expected, not an error.
📅 Q1 2025 – Q1 2026 · 5 quarters of data
ⓘ The newest quarter is usually incomplete when first published; states restate recent quarters in later CMS releases, so the latest figures typically revise upward. State coverage-policy changes can also shift quarter-to-quarter totals.
Prescriptions last 4 qtrs
2.6K
Units reimbursed last 4 qtrs
301.8K
Gross reimbursed last 4 qtrs
$60.2K
Avg / prescription
$23.60
Avg / unit
$0.1995
Latest quarter Q1 2026
628Rx
Medicaid pays / ea
$0.1995
gross reimbursed
vs
NADAC / ea
$0.1084
acquisition cost
=
Spread
+$0.0911
+84% vs cost
What Medicaid paid per ea (before rebates; includes the pharmacy’s dispensing fee) compared with NADAC — the average price pharmacies pay to buy the drug. A positive spread means Medicaid reimbursed more than the purchase price, before manufacturer rebates.
Fee-for-service vs managed care ⓘ
55% FFS 45% MCO
Fee-for-service · 1,415 Rx Managed care · 1,136 Rx
State Medicaid map
Alaska: no data reported AK Maine: no data reported ME Washington: 4,885 units · 62.5 per 100k residents WA Idaho: no data reported ID Montana: no data reported MT North Dakota: no data reported ND Minnesota: no data reported MN Wisconsin: no data reported WI Michigan: no data reported MI New York: no data reported NY Vermont: no data reported VT New Hampshire: no data reported NH Oregon: no data reported OR Nevada: 5,682 units · 178 per 100k residents NV Wyoming: no data reported WY South Dakota: no data reported SD Iowa: no data reported IA Illinois: no data reported IL Indiana: no data reported IN Ohio: no data reported OH Pennsylvania: no data reported PA New Jersey: no data reported NJ Massachusetts: no data reported MA California: 183,581 units · 471 per 100k residents CA Utah: no data reported UT Colorado: no data reported CO Nebraska: no data reported NE Missouri: no data reported MO Kentucky: no data reported KY West Virginia: no data reported WV Virginia: no data reported VA Maryland: no data reported MD Connecticut: no data reported CT Rhode Island: no data reported RI Arizona: 29,760 units · 400 per 100k residents AZ New Mexico: no data reported NM Kansas: no data reported KS Arkansas: no data reported AR Tennessee: no data reported TN North Carolina: no data reported NC South Carolina: no data reported SC Delaware: no data reported DE Oklahoma: no data reported OK Louisiana: 5,640 units · 123 per 100k residents LA Mississippi: no data reported MS Alabama: 660 units · 12.9 per 100k residents AL Georgia: no data reported GA D.C.: no data reported DC Hawaii: 9,384 units · 654 per 100k residents HI Texas: 15,480 units · 50.7 per 100k residents TX Florida: 46,696 units · 207 per 100k residents FL
Units reimbursed · per 100k residents
12.9654
gray = no data reported ⓘ
Colors are per 100,000 residents, so big states don’t automatically dominate. Tap or hover a state for its actual totals.
Tap or hover a state
…for its Medicaid breakdown
🏆 Top states by units · per 100k residents
1 Hawaii 654 /100k
2 California 471 /100k
3 Arizona 400 /100k
4 Florida 207 /100k
5 Nevada 178 /100k
6 Louisiana 123 /100k
7 Washington 62.5 /100k
8 Texas 50.7 /100k
National units — by quarter
💵 About the dollar figures: “reimbursed” is what Medicaid paid pharmacies before confidential manufacturer rebates, so the program’s real net cost is lower than these numbers. Fee-for-service and managed-care claims are combined unless split above. Source: CMS State Drug Utilization Data; per-100k rates use 2023 Census population estimates.

Medicaid utilization by pack size

Medicaid (SDUD) totals over the four most recent reported quarters for every package size of this drug — handy when a specific package (e.g. a starter/titration pack) carries little or no Medicaid volume on its own.
100 tablets this page65862-0621-01 2,551 Rx · $60,196
30 tablets65862-0621-30 No Medicaid data
1000 tablets65862-0621-99 No Medicaid data
12000 tablets65862-0621-53 No Medicaid data
Drug total (last 4 qtrs): 2,551 Rx · 301,768 units · $60,196 gross reimbursed
Tap a pack size to open its page. Source: CMS State Drug Utilization Data, last 4 quarters.

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

Medicare Part D (outpatient prescription) spending for Flecainide Acetate (matched by generic name) — the program that covers self-administered drugs. 9 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 Flecainide Acetate. 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
$11.61M
Claims incl. refills
336.2K
Beneficiaries
260.6K
Spend / beneficiary
$44.56
Spend / claim
$34.54
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

Listed for further processing / repackaging

What "drug for further processing" means

FDA lists this package under the "drug for further processing" marketing category: Aurobindo Pharma Limited supplies it to other companies for further processing or repackaging (blister cards that are later repackaged or co-packaged are a common example). The units themselves are a finished dosage form — which is why pricing or Medicaid data can still appear — but this exact package code may not be the presentation a retail pharmacy dispenses.

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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) ✓ Available
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
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) ✓ Available
“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

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Drug For Further Processing". Products approved under an application carry an NDA, ANDA, or BLA number.
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 Aurobindo Pharma Limited. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 30 tablets (65862-0621-30), 1000 tablets (65862-0621-99), 12000 tablets (65862-0621-53). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Aurobindo Pharma Limited 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.
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.
← 65862-0620-30 · Aurobindo 65862-0622-01 · Aurobindo →
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.