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donepezil hydrochloride 5 mg Tablet, Film Coated, 100-count — NDC 87063-0305-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

donepezil hydrochloride 5 mg Tablet, Film Coated, 100-count — NDC 87063-305-01 (Billing 87063-0305-01)

by ASCLEMED USA INC. · 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

This is a package of 100 tablets of donepezil hydrochloride 5 mg Tablet, Film Coated from ASCLEMED USA INC., marketed since Nov 2011 and currently FDA-listed. It is the main listing for this product, which comes in 5 package sizes.

NDC 87063-0305-01
🏷️ FDA NDC (as labeled) 87063-305-01 billing pads the product segment with a zero
This package
Contains100-count Pack sizes5 compare ↓
Main listing for product 87063-305 · Also comes in: 20 tablets 87063-305-20 30 tablets 87063-305-30 60 tablets 87063-305-60 90 tablets 87063-305-90
Rx only Generic 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 87063-305-01 alone.

Record
FDA NDC Directory package listing · Human prescription drug
Code segments
87063 labeler · 305 product · 01 package
Package marketed since
Sep 10, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8706330501 4
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87063-305-01
Product NDC 87063-305
11-digit billing NDC 87063030501
Application # ANDA200292
SPL Set ID 603c07bb-61bf-410f-8abf-01ef09d61c14
Established class (EPC) Cholinesterase Inhibitor
Mechanism of action Cholinesterase Inhibitors
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2011-11-01
Route ORAL
Dosage form TABLET, FILM COATED
Substance DONEPEZIL HYDROCHLORIDE
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 87063-305-01 — 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 → 87063-0305-01. 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
  • Unfortunately, no — donepezil doesn't cure Alzheimer's disease, and it won't stop the disease from progressing over time. What it can do is help manage symptoms like memory and thi...
  • Will donepezil cure my family member's Alzheimer's disease?
  • You should take donepezil once a day in the evening, just before going to bed. Food doesn't affect how well it's absorbed, so you can take it with or without a meal — whatever work...
  • When should I take donepezil, and does it matter if I take it with food?
📖 Read our full Donepezil 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 · 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: 20 tablets 30 tablets 60 tablets 90 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
87063-0305-01 You're viewing this Main listing 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2026-09-10 — Active
87063-0305-20 87063-305-20 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2026-09-10 — Active
87063-0305-30 87063-305-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2026-09-10 — Active
87063-0305-60 87063-305-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2026-09-10 — Active
87063-0305-90 87063-305-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2026-09-10 — Active

You're viewing the largest of 5 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 100-count package — 100 tablet, film coated in 1 bottle, plastic.
How does this package differ from NDC 87063-0305-20?
Both are donepezil hydrochloride 5 mg Tablet, Film Coated — the drug itself is identical. This page's package is the 100-count one, while NDC 87063-0305-20 is the 20 tablets package.
What NDC number is used to bill for this package of donepezil hydrochloride 5 mg Tablet, Film Coated?
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
Donepezil hydrochloride 5 mg 55111-0356-05 Dr. 500 tablets $0.044 AB Discontinued —
Donepezil Hydrochloride 5 mg 16571-0778-03 Rising 30 tablets $0.044 AB Availability likely —
Donepezil Hydrochloride 5 mg 33342-0027-07 Macleods 30 tablets $0.044 AB Availability likely —
Donepezil Hydrochloride 5 mg 71093-0127-01 ACI 30 tablets $0.044 — Discontinued —
Donepezil 5 mg 82009-0119-05 Quallent 500 tablets $0.044 AB Availability likely —
Donepezil Hydrochloride 5 mg 00904-6477-61 Major 1 tablet $0.044 AB Availability likely —
donepezil hydrochloride 5 mg 43547-0275-03 Solco 30 tablets $0.044 AB Availability likely —
Donepezil 5 mg 60687-0292-01 American 100 tablets $0.044 AB Availability likely —
Donepezil Hydrochloride 5 mg 62332-0092-10 Alembic 100 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 46708-0295-10 Alembic 100 tablets — AB FDA listed —
donepezil hydrochloride 5 mg 50090-3537-00 A-S 90 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 50090-6329-00 A-S 90 tablets — AB FDA listed —
Aricept 5 mg 62856-0245-30 Eisai 30 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 65862-0325-01 Aurobindo 100 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 71209-0019-01 Cadila 30 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 68788-8208-03 Preferred 30 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 00615-7951-05 NCS 15 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 70518-4392-00 REMEDYREPACK 90 tablets — AB FDA listed —
Donepezil 5 mg 31722-0737-01 Camber 100 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 50228-0139-10 ScieGen 1000 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 71335-2022-01 Bryant 90 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 60429-0321-10 Golden 1000 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 63629-9326-01 Bryant 90 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 68788-8711-03 Preferred 30 tablets — — FDA listed —
donepezil hydrochloride 5 mg 43547-0878-03 Solco 30 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 50090-7365-00 A-S 90 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 71335-2093-01 Bryant 90 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 13668-0102-05 Torrent 500 tablets — AB FDA listed —
Donepezil Hydrochloride 5 mg 71335-2065-01 Bryant 90 tablets — — Discontinued —
Donepezil Hydrochloride 5 mg 72162-2136-00 Bryant 1000 tablets — — Discontinued —
Donepezil Hydrochloride 5 mg 72189-0031-90 Direct_Rx 90 tablets — AB Discontinued —
donepezil hydrochloride 5 mg 29300-0248-01 Unichem 100 tablets — — FDA listed —
Donepezil Hydrochloride 5 mg 55154-7883-00 Cardinal 1 tablet — AB FDA listed —
Donepezil Hydrochloride 5 mg 67046-1476-03 Coupler 30 tablets — AB FDA listed —
Donepezil 5 mg 70518-4380-00 REMEDYREPACK 90 tablets — AB FDA listed —
donepezil hydrochloride 5 mgthis 87063-0305-01 ASCLEMED 100 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

🏛️
2011
On the market since
Nov 2011
📍
2026
Currently FDA-listed
15 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 blue / yellow
ShapeRound
ImprintHH210
Size8 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 Donepezil 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 M28OL1HH48
    Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
  • UNII L06K8R7DQK
    A synthetic blue dye approved by the FDA for use in medications and foods. It serves as a colorant to make pills and liquids visually distinct and easier to identify.
  • UNII 9XZ8H6N6OH
    A plant-based cellulose derivative used as a binder to hold tablet ingredients together, a thickener in liquids, and a coating agent to control how fast the medicine dissolves.
  • UNII 3NXW29V3WO
    Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
  • 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 3WJQ0SDW1A
    Polyethylene glycol is a synthetic liquid or solid polymer used in medicines as a solvent, lubricant, and humectant. It helps dissolve active ingredients, reduces friction during manufacturing, and retains moisture in the final product.
  • 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.
  • 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.

10 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

LabelerASCLEMED USA INC.
Application holderPRINSTON PHARMACEUTICAL INC
FDA applicationANDA200292 (ANDA)
Labeler code87063
First marketedNov 2011
Product typeHuman Prescription Drug
Portfolio136 products on file

More NDCs from ASCLEMED USA INC. labeler code 87063

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 ↗

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 ASCLEMED USA INC.. 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 4 other package presentations of this same product, including 20 tablets (87063-0305-20), 30 tablets (87063-0305-30), 60 tablets (87063-0305-60). 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?
ASCLEMED USA 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.
← 87063-0304-01 · ASCLEMED 87063-0306-01 · ASCLEMED →
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.