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Clonazepam .5 mg Tablet, 30-count — NDC 87441-0090-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Clonazepam .5 mg Tablet, 30-count — NDC 87441-090-01 (Billing 87441-0090-01)

by Unit Dose Solutions, Inc. · 30 TABLET in 1 BLISTER PACK

This is a package of 30 tablets of Clonazepam .5 mg Tablet from Unit Dose Solutions, Inc., marketed since Sep 2026 and currently FDA-listed. It is this product's only package size.

NDC 87441-0090-01
🏷️ FDA NDC (as labeled) 87441-090-01 billing pads the product segment with a zero
Rx only Generic On market CIV ⇄ 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

⚠️
Other active recalls for Clonazepam (different manufacturers) — 4 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class I · Nov 18, 2024 — Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. (Endo USA, Inc.) · FDA recall D-0179-2025
Class I · Nov 18, 2024 — Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. (Endo USA, Inc.) · FDA recall D-0181-2025
Class I · Nov 18, 2024 — Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. (Endo USA, Inc.) · FDA recall D-0178-2025
Class I · Nov 18, 2024 — Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. (Endo USA, Inc.) · FDA recall D-0180-2025
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) 87441-090-01
Product NDC 87441-090
11-digit billing NDC 87441009001
Application # ANDA074569
SPL Set ID 5c2ccdcf-4f47-df06-e063-6294a90a42eb
Established class (EPC) Benzodiazepine
Chemical class Benzodiazepines
DEA schedule CIV
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-09-24
Route ORAL
Dosage form TABLET
Substance CLONAZEPAM
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 87441-090-01 — 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 → 87441-0090-01. 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 treats certain seizure disorders and panic disorder. Your prescriber will tell you which applies to you.
  • Take it by mouth exactly as prescribed. Swallow regular tablets whole with water. If you have the orally disintegrating tablet, place it on your tongue with dry hands and let it di...
  • Please don't stop suddenly. Your body can become dependent, and abrupt stopping can cause serious withdrawal, including seizures. Your prescriber will lower the dose gradually.
  • Drowsiness, unsteadiness and dizziness are the most common. Let me know if you notice mood changes, depression, thoughts of self-harm, agitation or aggression, because those need p...
📖 Read our full Clonazepam guide →
1
Nutrient depletion considerations

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

🧪 Full Clonazepam 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.
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
87441-0090-01 You're viewing this Main listing 30 TABLET in 1 BLISTER PACK 2026-09-24 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Clonazepam .5 mg 00093-0832-01 Teva 100 tablets $0.020 AB Availability likely —
Clonazepam .5 mg 16729-0136-00 Accord 100 tablets $0.020 AB Availability likely —
Clonazepam .5 mg 59651-0722-01 Aurobindo 100 tablets $0.020 AB Availability likely —
Clonazepam .5 mg 62135-0769-90 Chartwell 90 tablets $0.020 AB Availability likely —
Clonazepam .5 mg 72888-0152-00 Advagen 1000 tablets $0.020 — Availability likely —
Clonazepam .5 mg 43547-0406-10 Solco 100 tablets $0.020 AB Availability likely —
Clonazepam .5 mg 00904-7227-61 Major 100 tablets $0.020 AB Availability likely —
Clonazepam .5 mg 50268-0173-15 AvPAK 50 tablets $0.020 AB Availability likely —
Clonazepam .5 mg 72603-0307-01 Northstar 100 tablets $0.020 — Availability likely —
Clonazepam .5 mg 60687-0861-01 American 100 tablets $0.020 AB Availability likely —
Klonopin .5 mg 61269-0605-10 H2-Pharma, 100 tablets $2.679 AB Availability likely —
Clonazepam .5 mg 63187-0226-30 Proficient 30 tablets — AB FDA listed —
Clonazepam .5 mg 63187-0603-30 Proficient 30 tablets — AB FDA listed —
Clonazepam .5 mg 58118-0832-08 Clinical 30 tablets — AB FDA listed —
Clonazepam .5 mg 63629-1202-01 Bryant 100 tablets — AB FDA listed —
Clonazepam .5 mg 63629-1203-01 Bryant 1000 tablets — AB FDA listed —
Clonazepam .5 mg 67544-0529-15 Aphena 15 tablets — AB FDA listed —
Clonazepam .5 mg 71205-0827-30 Proficient 30 tablets — AB FDA listed —
Clonazepam .5 mg 87441-0021-01 Unit 30 tablets — — FDA listed —
Clonazepam .5 mg 63629-1201-01 Bryant 500 tablets — AB FDA listed —
Clonazepam .5 mg 71335-0113-01 Bryant 20 tablets — AB Discontinued —
Clonazepam .5 mg 67046-1521-03 Coupler 30 tablets — — FDA listed —
Clonazepam .5 mg 70518-1801-00 REMEDYREPACK 100 tablets — AB FDA listed —
Clonazepam .5 mg 71335-2509-01 Bryant 20 tablets — — FDA listed —
Clonazepam .5 mg 71610-0790-10 Aphena 10 tablets — — FDA listed —
Clonazepam .5 mg 72162-1364-01 Bryant 100 tablets — AB FDA listed —
Clonazepam .5 mg 43063-0797-30 PD-Rx 30 tablets — AB FDA listed —
Clonazepam .5 mg 50090-2088-00 A-S 30 tablets — AB FDA listed —
Clonazepam .5 mg 70518-3960-00 REMEDYREPACK 100 tablets — AB FDA listed —
Clonazepam .5 mg 71610-0039-45 Aphena 45 tablets — AB FDA listed —
Clonazepam .5 mg 50090-4841-02 A-S 90 tablets — AB FDA listed —
Clonazepam .5 mg 58118-0152-08 Clinical 30 tablets — — FDA listed —
Clonazepam .5 mg 71610-0855-10 Aphena 10 tablets — AB FDA listed —
Clonazepam .5 mg 80425-0358-01 Advanced 30 tablets — AB FDA listed —
Clonazepam .5 mg 68071-4021-03 NuCare 30 tablets — AB FDA listed —
Clonazepam .5 mg 70518-3891-00 REMEDYREPACK 30 tablets — — FDA listed —
Clonazepam .5 mg 71610-0368-10 Aphena 10 tablets — AB FDA listed —
Clonazepam .5 mg 80425-0125-01 Advanced 30 tablets — AB FDA listed —
Clonazepam .5 mg 68788-8420-02 Preferred 20 tablets — AB FDA listed —
Clonazepam .5 mg 70518-2507-00 REMEDYREPACK 100 tablets — AB FDA listed —
Clonazepam .5 mg 70518-1297-01 REMEDYREPACK 100 tablets — AB FDA listed —
Clonazepam .5 mg 72189-0081-30 DIRECT 30 tablets — AB FDA listed —
Clonazepam .5 mg 80425-0402-01 Advanced 30 tablets — AB FDA listed —
Clonazepam .5 mg 71335-1810-01 Bryant 20 tablets — AB FDA listed —
Clonazepam .5 mg 72789-0307-30 PD-Rx 30 tablets — AB FDA listed —
Clonazepam .5 mg 55154-4318-00 Cardinal 10 tablets — AB FDA listed —
Clonazepam .5 mg 71610-0863-10 Aphena 10 tablets — AB FDA listed —
Clonazepam .5 mgthis 87441-0090-01 Unit 30 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

🏛️
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.

What it looks like

Color yellow
ShapeRound
Imprint832;TEVA
Size8 mm
ScoringScored — splits in 2
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 CQ3XH3DET6
    D&C Yellow No. 10 Aluminum Lake is a yellow colorant made by combining a dye with aluminum salts. It's used in medicines to add color for product identification and visual appeal.
  • UNII EWQ57Q8I5X
    Lactose monohydrate is a natural sugar derived from milk. It serves as a filler and binder in tablets and capsules, helping create the proper size, texture, and consistency of the medicine.
  • 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 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 RDH86HJV5Z
    Povidone K90 is a synthetic polymer made from a chemical called vinyl pyrrolidone. It acts as a binder to hold pill ingredients together and as a dispersant to help the medicine break down and dissolve properly in your body.
  • 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

LabelerUnit Dose Solutions, Inc.
Application holderTEVA PHARMACEUTICALS USA INC
FDA applicationANDA074569 (ANDA)
Labeler code87441
First marketedSep 2026
DEA scheduleCIV
Product typeHuman Prescription Drug
Portfolio87 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 Clonazepam — the program that covers self-administered drugs. 10 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 Clonazepam. 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
$15.53M
Claims incl. refills
2.1M
Beneficiaries
936.4K
Spend / beneficiary
$16.58
Spend / claim
$7.45
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 Unit Dose Solutions, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Unit Dose Solutions, Inc. 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.
← 87441-0089-01 · Unit 87441-0091-01 · Unit →
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.