Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Nicotine Patches 21 mg/1001 Patch, 30 patches — NDC 85795-002-01 (Billing 85795-0002-01)
by Shenzhen TeLaFaErJiaLuo Technology Co., Ltd. · 30 PATCH in 1 BOX
This is a package of 30 patches of Nicotine Patches 21 mg/1001 Patch from Shenzhen TeLaFaErJiaLuo Technology Co., Ltd., marketed since Jul 2025 and currently FDA-listed. It is this product's only package size.
NDC 85795-0002-01
🏷️ FDA NDC (as labeled)
85795-002-01
billing pads the product segment with a zero
🗂️ FDA directory synced Oct 1, 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 →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
85795-002-01
Product NDC
85795-002
11-digit billing NDC
85795000201
RxCUI
198030
UNII
6M3C89ZY6R
Application #
M017
SPL Set ID
3a1abd26-c0aa-8a65-e063-6294a90ab66e
Established class (EPC)
Cholinergic Nicotinic Agonist
Chemical class
Nicotine
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2025-07-17
Route
TOPICAL
Dosage form
PATCH
Substance
NICOTINE
Quick answers
- RxCUI (RxNorm): 198030
Why two NDCs?
The FDA registers this code as 85795-002-01 — 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 → 85795-0002-01. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Cholinergic Nicotinic Agonist class.
Pharmacologic class
Cholinergic Nicotinic Agonist
Drug family (ATC)
Drugs used in nicotine dependence
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.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
📗 Our plain-language guide HelloPharmacist
- That's a really common concern, and it's worth addressing. Nicotine replacement products do deliver nicotine, but in a much more controlled way — without the tar, carbon monoxide,...
- What exactly does nicotine replacement do — isn't it just replacing one nicotine habit with another?
- Yes, it actually does matter. If you typically smoke your first cigarette within 30 minutes of waking up, your nicotine dependence is likely stronger, so you'd use the higher-stren...
- How do I know which strength to use — and does it matter when I have my first cigarette in the morning?
Patient education
Supplement & herbal interactions
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about Nicotine Patches?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per each | Per 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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 2, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 85795-0002-01 You're viewing this Main listing | 30 PATCH in 1 BOX | 2025-07-17 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Nicotine 21 mg/24h 70677-0032-01 | Strategic | 14 pouches | $1.533 | — | FDA listed | — |
| Nicotine transdermal system step 1 21 mg/24h 00536-1108-88 | Rugby | 14 patches | $1.873 | — | Availability likely | — |
| Nicotine 21 mg/24h 00536-5896-53 | Rugby | 7 pouches | $1.873 | — | Availability likely | — |
| Nicotine transdermal system step 1 21 mg/24h 43598-0448-28 | Dr. | 28 patches | $1.873 | — | Discontinued | — |
| Nicotine Transdermal System 21 mg/24h 46122-0353-74 | AmerisourceBergen | 14 pouches | $1.873 | — | Availability likely | — |
| Nicotine Transdermal System 21 mg/24h 46122-0568-03 | AmerisourceBergen | 28 pouches | $1.873 | — | Availability likely | — |
| Nicotine Transdermal System 21 mg/24h 50742-0670-07 | Ingenus | 7 pouches | $1.873 | — | Availability likely | — |
| Nicotine Transdermal System 21 mg/24h 68001-0434-88 | BluePoint | 7 pouches | $1.873 | — | Availability likely | — |
| Nicotine Transdermal System Patch Step 1 21 mg/24h 68001-0699-88 | BluePoint | 7 patches | $1.873 | — | Availability likely | — |
| Nicotine Transdermal System 21 mg/24h 70000-0512-01 | Cardinal | 7 pouches | $1.873 | — | Availability likely | — |
| Nicotine Transdermal System step 1 21 mg/24h 70000-0762-01 | CARDINAL | 7 patches | $1.873 | — | Availability likely | — |
| foster and thrive STEP 1 21 mg/24h 70677-1182-01 | Strategic | 14 pouches | $1.873 | — | Availability likely | — |
| Nicotine transdermal system step 1 21 mg/24h 70677-1266-01 | Strategic | 14 patches | $1.873 | — | Availability likely | — |
| Nicotine Transdermal System 21 mg/24h 76282-0783-40 | EXELAN | 14 pouches | $1.873 | — | Availability likely | — |
| Nicoderm Cq 21 mg/24h 00135-0194-01 | Haleon | 7 patches | — | — | FDA listed | — |
| Nicotine transdermal system step 1 21 mg/24h 00363-0455-70 | Walgreens | 7 patches | — | — | FDA listed | — |
| Nicotine Transdermal System 21 mg/24h 00363-1245-01 | Walgreens | 14 pouches | — | — | FDA listed | — |
| Nicotine Transdermal System 21 mg/24h 03215-0122-14 | Aveva | 14 patches | — | — | FDA listed | — |
| Nicotine Transdermal System 21 mg/24h 03215-1203-07 | Aveva | 7 pouches | — | — | FDA listed | — |
| Nicotine transdermal system 21 mg/24h 11673-0194-01 | Target | 7 patches | — | — | Discontinued | — |
| Nicotine transdermal system step 1 21 mg/24h 11822-4975-00 | Rite | 7 patches | — | — | FDA listed | — |
| Nicotine Transdermal System 21 mg/24h 36800-0038-14 | Topco | 14 pouches | — | — | FDA listed | — |
| Nicotine Transdermal System 21 mg/24h 37808-0461-01 | H-E-B | 14 pouches | — | — | FDA listed | — |
| Nicotine transdermal system 21 mg/24h 49035-0194-01 | Wal-Mart | 7 patches | — | — | FDA listed | — |
| Nicotine 21 mg/24h 50090-1697-00 | A-S | 14 pouches | — | — | FDA listed | — |
| Nicotine Transdermal System 21 mg/24h 50090-7936-00 | A-S | 14 patches | — | — | FDA listed | — |
| Medline 21 mg 53329-0192-89 | Medline | 14 patches | — | — | FDA listed | — |
| Habitrol Step 1 21 mg/24h 55741-0448-28 | Dr. | 28 patches | — | — | FDA listed | — |
| Nicotine transdermal system step 1 21 mg/24h 55910-0313-02 | DOLGENCORP, | 2 patches | — | — | FDA listed | — |
| Nicotine transdermal system step 1 21 mg/24h 59450-0003-74 | The | 14 patches | — | — | FDA listed | — |
| Nicotine transdermal system step 1 21 mg/24h 59779-0448-02 | CVS | 2 pouches | — | — | FDA listed | — |
| Nicotine transdermal system step 1 21 mg/24h 60429-0445-14 | Golden | 14 patches | — | — | FDA listed | — |
| Nicotine transdermal system step 1 21 mg/24h 63868-0735-14 | Chain | 14 patches | — | — | FDA listed | — |
| Nicotine 21 mg/24h 79481-0052-01 | Meijer, | 14 pouches | — | — | FDA listed | — |
| Sielkin QUIT SMOKING NICOTINE PATCHES 21mg 21 mg/g 83364-0017-01 | YITONGBADA | 30 patches | — | — | FDA listed | — |
| Sefudun Quit Smoking Nicotine Patches 21 mg 83804-0001-01 | Shenzhen | 30 patches | — | — | FDA listed | — |
| NWRB Nicotine Transdermal Patch 21 mg 84288-0007-01 | Dongkou | 30 patches | — | — | FDA listed | — |
| Nicotine Transdermal System 21 mg/24h 84720-0122-14 | Quitine | 14 patches | — | — | FDA listed | — |
| QUIT SMOKING Proven Patches 21 mg/g 84867-0013-01 | Jiashen | 30 patches | — | — | FDA listed | — |
| Rstrvbr QUIT SMOKING 21 mg/1001 85248-0130-01 | Jiangxi | 30 patches | — | — | FDA listed | — |
| Serynth Nicotine Transdermal Stop Smoking Aid 21 mg/1001 85248-0164-01 | Jiangxi | 21 patches | — | — | FDA listed | — |
| Nicotine Patches 21 mg/21mg 85333-0003-02 | Zhejiang | 14 patches | — | — | FDA listed | — |
| Nicotine Patches 21 mg/1001this 85795-0002-01 | Shenzhen | 30 patches | — | — | FDA listed | — |
| WOFANLI Quit Smoking Nicotine Patches 21 mg/1001 85835-0004-01 | Shenzhen | 30 patches | — | — | FDA listed | — |
| WOFANLI Quit Smoking Nicotine Patches 21 mg/1001 85835-0009-01 | Shenzhen | 30 patches | — | — | FDA listed | — |
| NicDuic Quit Smoking Nicotine Patches 1 Step 21 mg/1001 85835-0012-01 | Shenzhen | 30 patches | — | — | FDA listed | — |
| NicDuic Quit Smoking Nicotine Patches 1-3 Step 21 mg/1001 85835-0013-01 | Shenzhen | 30 patches | — | — | FDA listed | — |
| quit smoking patches 21 mg 87135-0001-01 | Henan | 30 patches | — | — | FDA listed | — |
| GUHIO Nicotine Patch 21 mg 87278-0001-01 | Guangxi | 42 patches | — | — | FDA listed | — |
| Nicotine Stop Smoking AID 21 mg 87278-0002-01 | Guangxi | 60 patches | — | — | FDA listed | — |
| Nicotine Stop Smoking AID 21 mg 87278-0009-01 | Guangxi | 60 patches | — | — | FDA listed | — |
| Hqlsey Quit Smoking Patches 21 mg/1001 87405-0001-01 | Hansen | 14 patches | — | — | FDA listed | — |
| Nicotine Patch 21 mg 87704-0004-01 | Guangzhou | 30 patches | — | — | 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2025
On the market since
Jul 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found
We did not find an FDA-approved generic match for this exact strength, form and route.
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.
- FDA Orange Book · refreshed Sep 3, 2026
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 J94PBK7X8S
A synthetic polymer derived from acrylic acid monomers. In medicines, it's used as a binder to hold tablet ingredients together and sometimes as a coating agent to control where and how the drug releases in the body.
-
UNII 3K9958V90M
A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
-
UNII CPD4NFA903
Aluminum is a metallic element used in pharmaceuticals as a colorant and opacifying agent. It reflects light to create a white or silvery appearance in tablets, capsules, and coatings.
-
UNII 213N3S8275
A natural compound extracted from camphor tree wood or made synthetically. It's used in medicines as a flavoring agent and to provide a cooling or soothing sensation in topical products.
-
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 SMD1X3XO9M
Powdered cellulose is a fine, plant-based powder made from purified wood fibers. In medicines, it acts as a filler to add bulk and volume, and helps tablets or capsules hold together during manufacturing and storage.
6 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statescamphor, ethanol, acrylate adhesive, aluminized polyester, cellulose paper, methacryic acid copolymer
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerShenzhen TeLaFaErJiaLuo Technology Co., Ltd.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code85795
First marketedJul 2025
Product typeHuman Otc Drug
Portfolio3 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Do Not Use
📄 Ask a Doctor Before Use If
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Use reduces withdrawal symptoms, including nicotine cravings associated with quitting smoking.
⏱️ Dosage and Administration ▾
Directions if you are under 18 years of age,ask a doctor before use. Before use,carefully read the insert for complete instructions. Ifyou smoke more than 10 cigarettes per day,follow this 10-week schedule: lf you smoke 10 or fewer cigarettes per day,skip STEP1(21 mg).Start with STEP 2(14 mg)for 6 weeks-using two 14 mg patches per day for the first week,then one 14 mg patch per day for weeks 2 to 6.Then move to STEP3(7mg)for 2 weeks,and stop.
⚠️ Warnings ▾
Warnings For external use only
📦 Storage and Handling ▾
Other information Store at 20-25°℃(68-77°F)
🧪 Active Ingredient ▾
Active Ingredient Nicotine 21mg
🧪 Inactive Ingredients ▾
Inactive ingredients camphor , ethanol , acrylate adhesive , aluminized polyester , cellulose paper , methacryic acid copolymer
🎯 Purpose ▾
Purpose Stop smoking aid
📄 Do Not Use ▾
Do not use heart disease , high blood pressure , skin sensitivity or rash , diabetes , history of seizures
📄 Ask a Doctor Before Use If ▾
Ask Doctor using a non-nicotine stop smoking drug , pregnant or breast-feeding
📄 When Using This Product ▾
When Using if you have vivid dreams or other sleep disturbances remove this patch at bedtime
📄 Stop Use and Ask a Doctor If ▾
Stop Use if irritation or allergic reactions occur
📄 Keep Out of Reach of Children ▾
Keep Out Of Reach Of Children In case of accidental ingestion,seek medical advice immediatelyor contact aPoison Control Center(1-800-222-1222)
📄 Questions or Comments ▾
Questions Contactus at:[email protected]
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL 1
No label section mentions that — try another word, or open the full label on DailyMed below.
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
Over-the-counter (OTC) 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 | — 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) | — 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
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 "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
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 Shenzhen TeLaFaErJiaLuo Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Shenzhen TeLaFaErJiaLuo Technology Co., Ltd. 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 an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
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.
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.