Home › NDC Lookup › Ingredients › Tamsulosin Hydrochloride › 65841-0695-06
Tamsulosin Hydrochloride .4 mg Capsule, 30-count — NDC 65841-0695-06 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Tamsulosin Hydrochloride .4 mg Capsule, 30-count — NDC 65841-695-06 (Billing 65841-0695-06)

by Zydus Lifesciences Limited · 30 CAPSULE in 1 BOTTLE

This is a package of 30 capsules of Tamsulosin Hydrochloride .4 mg Capsule from Zydus Lifesciences Limited, marketed since Apr 2010 and currently FDA-listed.

NDC 65841-0695-06
🏷️ FDA NDC (as labeled) 65841-695-06 billing pads the product segment with a zero
This package
Contains30-count Pack sizes7 compare ↓
Also priced by: Part D plans $0.1304/unit — full pricing hub ↓
Product page 65841-0695-01 Also comes in: 60 capsules 65841-695-14 90 capsules 65841-695-16 100 capsules 65841-695-01 100 capsules 65841-695-77 500 capsules 65841-695-05 1000 capsules 65841-695-10
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 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 65841-695-06 alone.

Record
FDA NDC Directory package listing · Human prescription drug
Code segments
65841 labeler · 695 product · 06 package
Package marketed since
Apr 27, 2010
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6584169506 9
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 65841-695-06
Product NDC 65841-695
11-digit billing NDC 65841069506
RxCUI 863669
UNII 11SV1951MR
Application # ANDA078225
SPL Set ID 276c7e26-f86a-46b9-b626-ceef76b729a4
Established class (EPC) alpha-Adrenergic Blocker
Mechanism of action Adrenergic alpha-Antagonists
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2010-04-27
Route ORAL
Dosage form CAPSULE
Substance TAMSULOSIN HYDROCHLORIDE
TE code (Orange Book) AB · RLD · RS
Quick answers
  • RxCUI (RxNorm): 863669
Why two NDCs? The FDA registers this code as 65841-695-06 — 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 → 65841-0695-06. 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.

RxNorm drug class

This medicine belongs to the alpha-Adrenergic Blocker class.

Pharmacologic class alpha-Adrenergic Blocker
Drug family (ATC) Alpha-adrenoreceptor antagonists
How it works Adrenergic alpha-Antagonists
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📗 Our plain-language guide HelloPharmacist
  • Tamsulosin is designed to ease the urinary symptoms caused by an enlarged prostate — things like a weak stream, straining to start, or feeling like you haven't fully emptied your b...
  • What exactly is tamsulosin supposed to do for me?
  • Take it once a day, about 30 minutes after the same meal each day — for example, every morning after breakfast. Consistency matters here. Swallow the capsule whole; don't crush, ch...
  • It can, yes — this is one of the more common side effects, and it's worth knowing about upfront. Some men notice reduced ejaculation volume or what's called retrograde ejaculation,...
📖 Read our full Tamsulosin 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 eachPer 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 · Q2 2026 $0.1304 $3.91 / 30 capsules
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
65841-0695-01 65841-695-01 Main listing 100 CAPSULE in 1 BOTTLE 2010-04-27 — Active
65841-0695-05 65841-695-05 500 CAPSULE in 1 BOTTLE 2010-04-27 — Active
65841-0695-06 You're viewing this 30 CAPSULE in 1 BOTTLE 2010-04-27 — Active
65841-0695-10 65841-695-10 1000 CAPSULE in 1 BOTTLE 2010-04-27 — Active
65841-0695-14 65841-695-14 60 CAPSULE in 1 BOTTLE 2010-04-27 — Active
65841-0695-16 65841-695-16 90 CAPSULE in 1 BOTTLE 2010-04-27 — Active
65841-0695-77 65841-695-77 10 BLISTER PACK in 1 CARTON / 10 CAPSULE in 1 BLISTER PACK 2010-04-27 — Active

Pack size FAQ

What quantity is in this package?
This is a 30-count package — 30 capsule in 1 bottle.
How does this package differ from NDC 65841-0695-14?
Both are Tamsulosin Hydrochloride .4 mg Capsule — the drug itself is identical. This page's package is the 30-count one, while NDC 65841-0695-14 is the 60 capsules package.
What NDC number is used to bill for this package of Tamsulosin Hydrochloride .4 mg Capsule?
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.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Tamsulosin Hydrochloride .4 mg 00904-7383-61 Major 100 capsules $0.050 AB Availability likely —
Tamsulosin Hydrochloride .4 mg 50268-0740-15 AvPAK 50 capsules $0.050 AB Availability likely —
Tamsulosin Hydrochloride .4 mg 57237-0014-01 Rising 100 capsules $0.050 AB Availability likely —
Tamsulosin Hydrochloride .4 mg 62135-0775-30 Chartwell 30 capsules $0.050 AB Availability likely —
Tamsulosin Hydrochloride .4 mg 65862-0598-01 Aurobindo 100 capsules $0.050 — Availability likely —
Tamsulosin Hydrochloride .4 mg 67877-0450-01 Ascend 100 capsules $0.050 AB Availability likely —
Tamsulosin Hydrochloride .4 mg 68084-0299-01 American 100 capsules $0.050 AB Availability likely —
Tamsulosin Hydrochloride .4 mg 68382-0132-01 Zydus 100 capsules $0.050 AB Availability likely —
Tamsulosin Hydrochloride .4 mg 72603-0115-01 NorthStar 100 capsules $0.050 AB Availability likely —
Tamsulosin hydrochloride .4 mg 76282-0744-05 EXELAN 500 capsules $0.050 AB Availability likely —
Tamsulosin Hydrochloride .4 mg 82009-0025-10 Quallent 1000 capsules $0.050 AB Availability likely —
tamsulosin hydrochloride .4 mg 00781-2076-01 Sandoz 100 capsules $0.054 — FDA listed —
Tamsulosin Hydrochloride .4 mg 00115-8211-01 Amneal 100 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 00615-8055-05 NCS 15 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 33342-0159-07 Macleods 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 42291-0989-10 AvKARE 1000 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 43063-0725-30 PD-Rx 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 43063-0947-30 PD-Rx 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 50090-1846-00 A-S 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 50090-3646-00 A-S 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 50090-4906-00 A-S 90 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 50090-5553-00 A-S 90 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 50090-6699-00 A-S 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 50090-6700-00 A-S 90 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 51407-0879-90 Golden 90 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 51655-0832-52 Northwind 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 55154-2142-00 Cardinal 10 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 55154-2636-00 Cardinal 10 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 60760-0598-90 St. 90 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 61919-0703-90 DIRECT 5904900000 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 62756-0160-08 Sun 100 capsules — — FDA listed —
Tamsulosin Hydrochloride .4 mg 63187-0358-07 Proficient 7 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 63187-0371-07 Proficient 7 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 63187-0469-30 Proficient 30 capsules — — FDA listed —
Tamsulosin Hydrochloride .4 mg 63629-4346-01 Bryant 30 capsules — AB FDA listed —
Tamsulosin hydrochloride .4 mg 63672-0021-09 Synthon 20000 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mgthis 65841-0695-06 Zydus 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 67046-1015-03 Coupler 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 67296-2220-01 Redpharm 7 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 68071-1840-01 NuCare 100 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 68071-2561-01 NuCare 10 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 68071-4443-01 NuCare 10 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 68071-4872-09 NuCare 90 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 68071-5118-01 NuCare 100 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 68788-7050-01 Preferred 100 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 70518-0179-00 REMEDYREPACK 30 capsules — AB Discontinued —
Tamsulosin Hydrochloride .4 mg 70518-2052-00 REMEDYREPACK 90 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 71205-0217-07 Proficient 7 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 71205-0688-07 Proficient 7 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 71335-0398-01 Bryant 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 71335-1538-01 Bryant 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 71335-1784-01 Bryant 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 71610-0724-30 Aphena 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 71610-0738-30 Aphena 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 71610-0835-30 Aphena 30 capsules — AB FDA listed —
Tamsulosin hydrochloride .4 mg 71610-0910-30 Aphena 30 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 72162-2217-05 Bryant 500 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 72162-2502-00 Bryant 1000 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 72162-2509-01 Bryant 100 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 72865-0282-01 XLCare 100 capsules — AB FDA listed —
tamsulosin hydrochloride .4 mg 72865-0350-05 XLCare 500 capsules — AB FDA listed —
Tamsulosin Hydrochloride .4 mg 68788-4145-01 Preferred 100 capsules — AB 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

🏛️
2010
On the market since
Apr 2010
📍
2026
Currently FDA-listed
16 years listed
🔓
·
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.

What it looks like

Color Green / Orange
ShapeCapsule
ImprintZA;18;0;4mg
Size18 mm
ScoringNot scored
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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 Tamsulosin 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.

  • UNII OP1R32D61U
    Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
  • UNII 35SW5USQ3G
    A synthetic yellow dye used to color medicines. It helps make tablets, capsules, and liquids visually distinct so patients can easily identify their medication.
  • UNII H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • UNII WZB9127XOA
    A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
  • UNII H77VEI93A8
    A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
  • UNII EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • UNII 2G86QN327L
    Gelatin is a protein derived from animal collagen, commonly used in medicines as a gelling agent and capsule material. It helps create soft or hard capsule shells that hold and release medication, and can also thicken liquid formulations.
  • UNII 1CS02G8656
    Methacrylic acid is a synthetic polymer used as a coating material and binder in tablets and capsules. It helps control how and where the medication releases in the digestive system.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • UNII XHX3C3X673
    Triacetin is a clear, oily liquid made from glycerin and acetic acid. It works as a plasticizer and solvent in medicines, helping soften coatings and improve how liquids mix together in formulations.

13 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

LabelerZydus Lifesciences Limited
Application holderZYDUS PHARMACEUTICALS USA INC
FDA applicationANDA078225 (ANDA)
Labeler code65841
First marketedApr 2010
Product typeHuman Prescription Drug
Portfolio720 products on file

More NDCs from Zydus Lifesciences Limited labeler code 65841

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.
📄 Package Label / Principal Display Panel
📄 Package Label / Principal Display Panel 27 words ▾

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 65841-695-01 in bottle of 100 Capsules Tamsulosin Hydrochloride Capsules USP, 0.4 mg R x only 100 Capsules tamsulosin hcl capsules, 0.4 mg

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

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 Zydus Lifesciences 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 6 other package presentations of this same product, including 60 capsules (65841-0695-14), 90 capsules (65841-0695-16), 100 capsules (65841-0695-01). 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?
Zydus Lifesciences 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.
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.
← 65841-0693-01 · Zydus 65841-0705-01 · Zydus →
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.