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Atenolol 100 mg Tablet, 180-count — NDC 71335-3178-06 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Atenolol 100 mg Tablet, 180-count — NDC 71335-3178-6 (Billing 71335-3178-06)

by Bryant Ranch Prepack · 180 TABLET in 1 BOTTLE

This is a package of 180 tablets of Atenolol 100 mg Tablet from Bryant Ranch Prepack, marketed since Dec 2007 and currently FDA-listed.

NDC 71335-3178-06
🏷️ FDA NDC (as labeled) 71335-3178-6 billing pads the package segment with a zero
This package
Contains180-count Pack sizes7 compare ↓
Product page 71335-3178-01 Also comes in: 10 tablets 71335-3178-7 20 tablets 71335-3178-5 30 tablets 71335-3178-2 60 tablets 71335-3178-3 90 tablets 71335-3178-4 100 tablets 71335-3178-1
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 2, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 71335-3178-6
Product NDC 71335-3178
11-digit billing NDC 71335317806
Application # ANDA077877
SPL Set ID 7836ee53-902b-4a3e-9523-6d4311cfba0e
Established class (EPC) beta-Adrenergic Blocker
Mechanism of action Adrenergic beta-Antagonists
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2007-12-04
Route ORAL
Dosage form TABLET
Substance ATENOLOL
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 71335-3178-6 — a 5-4-1 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 package segment → 71335-3178-06. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It treats high blood pressure and helps manage long-term angina. It is also used in people who are stable after a definite or suspected heart attack to lower the risk of death from...
  • Atenolol tablets are swallowed by mouth, usually once a day. Take it as your prescriber and the label direct. Your doctor may adjust the dose based on how you respond.
  • Please don't stop it suddenly. Stopping abruptly can make angina worse and has led to heart attacks and dangerous heart rhythms. Talk to your doctor first so they can guide you.
  • Tiredness, dizziness, cold hands and feet, and a slower heartbeat are the more common ones. Most are mild and pass. Call your doctor for fainting, wheezing, swelling, worsening bre...
📖 Read our full Atenolol guide →
1
Nutrient depletion considerations

Atenolol may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Atenolol nutrient depletion report →
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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 · 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.
Try another pack size: 10 tablets 20 tablets 30 tablets 60 tablets 90 tablets 100 tablets
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
71335-3178-01 71335-3178-1 Main listing 100 TABLET in 1 BOTTLE 2026-09-24 — Active
71335-3178-02 71335-3178-2 30 TABLET in 1 BOTTLE 2026-09-24 — Active
71335-3178-03 71335-3178-3 60 TABLET in 1 BOTTLE 2026-09-24 — Active
71335-3178-04 71335-3178-4 90 TABLET in 1 BOTTLE 2026-09-24 — Active
71335-3178-05 71335-3178-5 20 TABLET in 1 BOTTLE 2026-09-24 — Active
71335-3178-06 You're viewing this 180 TABLET in 1 BOTTLE 2026-09-24 — Active
71335-3178-07 71335-3178-7 10 TABLET in 1 BOTTLE 2026-09-24 — Active

You're viewing the largest of 7 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 180-count package — 180 tablet in 1 bottle.
How does this package differ from NDC 71335-3178-07?
Both are Atenolol 100 mg Tablet — the drug itself is identical. This page's package is the 180-count one, while NDC 71335-3178-07 is the 10 tablets package.
What NDC number is used to bill for this package of Atenolol 100 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.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Atenolol 100 mg 83980-0024-01 Ipca 100 tablets $0.036 AB Availability likely —
Atenolol 100 mg 29300-0412-01 Unichem 100 tablets $0.036 AB Availability likely —
Atenolol 100 mg 00093-0753-01 Teva 100 tablets $0.036 AB Availability likely —
Atenolol 100 mg 64980-0439-01 Rising 100 tablets $0.036 AB Availability likely —
Atenolol 100 mg 65862-0170-01 Aurobindo 100 tablets $0.036 AB Availability likely —
Atenolol 100 mg 68382-0024-01 Zydus 100 tablets $0.036 AB Availability likely —
Atenolol 100 mg 00378-0757-01 Mylan 100 tablets $0.036 AB Availability likely —
Atenolol 100 mg 51079-0685-20 Mylan 100 tablets $0.036 AB Availability likely —
Atenolol 100 mg 43353-0986-60 Aphena 90 tablets — AB FDA listed —
Atenolol 100 mg 50090-5738-00 A-S 30 tablets — AB FDA listed —
Atenolol 100 mg 68071-4751-09 NuCare 90 tablets — AB FDA listed —
Atenolol 100 mg 68788-4112-01 Preferred 100 tablets — AB FDA listed —
Atenolol 100 mg 87063-0179-01 ASCLEMED 100 tablets — AB FDA listed —
Atenolol 100 mg 51655-0736-26 Northwind 90 tablets — AB FDA listed —
Tenormin 100 mg 52427-0431-90 Almatica 90 tablets — AB Discontinued —
Atenolol 100 mg 60429-0026-10 Golden 1000 tablets — AB FDA listed —
Atenolol 100 mg 68071-5162-01 NuCare 100 tablets — AB FDA listed —
Atenolol 100 mg 72162-2326-00 Bryant 1000 tablets — AB FDA listed —
Atenolol 100 mg 50090-6311-00 A-S 30 tablets — AB FDA listed —
Atenolol 100 mg 51655-0104-26 Northwind 90 tablets — AB FDA listed —
Atenolol 100 mg 48433-0006-20 Safecor 100 tablets — AB FDA listed —
Atenolol 100 mg 65841-0024-01 Zydus 100 tablets — AB FDA listed —
Atenolol 100 mg 66267-0029-30 NuCare 30 tablets — AB FDA listed —
Atenolol 100 mg 68788-7535-01 Preferred 100 tablets — AB FDA listed —
Tenormin 100 mg 24979-0246-07 Upsher-Smith 90 tablets — AB FDA listed —
Atenolol 100 mg 68071-3851-03 NuCare 30 tablets — AB FDA listed —
Atenolol 100 mg 71335-2531-01 Bryant 100 tablets — AB FDA listed —
Atenolol 100 mg 71335-2774-01 Bryant 100 tablets — AB FDA listed —
Atenolol 100 mg 67046-1076-03 Coupler 30 tablets — AB FDA listed —
Atenolol 100 mg 70518-4099-00 REMEDYREPACK 90 tablets — AB FDA listed —
Atenolol 100 mg 71335-1264-01 Bryant 100 tablets — AB Discontinued —
atenolol 100 mg 72189-0152-90 direct 90 tablets — AB FDA listed —
Atenolol 100 mg 60760-0642-90 St 90 tablets — AB FDA listed —
Atenolol 100 mg 50090-8048-00 A-S 30 tablets — AB FDA listed —
Atenolol 100 mgthis 71335-3178-06 Bryant 180 tablets — 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

🏛️
2007
On the market since
Dec 2007
📍
2026
Currently FDA-listed
19 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 White
ShapeRound
ImprintRE;21
Size9 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.

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

  • UNII 0E53J927NA
    Magnesium carbonate is a mineral powder used in medicines as a filler to add bulk and as a buffer to help regulate acidity in the formulation.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • UNII 5856J3G2A2
    A starch-based powder made from potatoes and processed with sodium. It acts as a disintegrant, helping the tablet or capsule break apart quickly in the stomach so the medicine can be absorbed.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.

6 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

LabelerBryant Ranch Prepack
Application holderIPCA LABORATORIES LTD
FDA applicationANDA077877 (ANDA)
Labeler code71335
First marketedDec 2007
Product typeHuman Prescription Drug
Portfolio4,436 products on file
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 Atenolol — 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 Atenolol. 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
$11.45M
Claims incl. refills
1.4M
Beneficiaries
1.2M
Spend / beneficiary
$9.84
Spend / claim
$7.99
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 Bryant Ranch Prepack. 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 10 tablets (71335-3178-07), 20 tablets (71335-3178-05), 30 tablets (71335-3178-02). 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?
Bryant Ranch Prepack 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.
← 71335-3177-01 · Bryant 71335-3179-01 · Bryant →
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.