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Scopolamine 1 mg/3d Patch, Extended Release — NDC 70771-1787-02 package photo

Scopolamine 1 mg/3d Patch, Extended Release

by Zydus Lifesciences Limited · 10 POUCH in 1 CARTON (70771-1787-2) / 1 PATCH in 1 POUCH / 3 d in 1 PATCH
NDC 70771-1787-02
🏷️ FDA NDC (as labeled) 70771-1787-2 billing pads the package segment with a zero
This package
Contains3 d in 1 patch Pack sizes3 compare ↓
Also priced by: Part D plans $8.13/unit — full pricing hub ↓
Rx only Generic On market Non-controlled
🗂️ Data synced 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

FDA NDC (as labeled) 70771-1787-2
Product NDC 70771-1787
11-digit billing NDC 70771178702
RxCUI 226552
UNII DL48G20X8X
Application # ANDA217893
SPL Set ID 016df9f3-61d5-45e9-b1d6-791a5d2f26d5
Established class (EPC) Anticholinergic
Mechanism of action Cholinergic Antagonists
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-09-05
Route TRANSDERMAL
Dosage form PATCH, EXTENDED RELEASE
Substance SCOPOLAMINE
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 70771-1787-2 — 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 → 70771-1787-02. 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 Anticholinergic class.

Pharmacologic class Anticholinergic
Drug family (ATC) Other antiemetics, Other hypnotics and sedatives, Anticholinergics
How it works Cholinergic 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.

🏭 Manufacturer & labeler

LabelerZydus Lifesciences Limited
Application holderZYDUS PHARMACEUTICALS USA INC
FDA applicationANDA217893 (ANDA)
Labeler code70771
First marketedSep 2024
Product typeHuman Prescription Drug
Portfolio717 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.

🩺 Clinical

📖 What it is MedlinePlus · NLM

Scopolamine is used to prevent nausea and vomiting caused by motion sickness or medications used during surgery. Scopolamine is in a class of medications called antimuscarinics. It works by blocking the effects of a certain natural substance (acetylcholine) on the central nervous system.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • Apply it to the hairless skin directly behind one ear — that flat area just behind the earlobe. Either side works fine. The key is that the skin is clean, dry, and hair-free so the...
  • Where exactly do I put the patch, and does it matter which side?
  • Put it on at least 4 hours before you need it to be working — so if you're boarding a cruise ship in the morning, apply it the night before. The patch takes several hours to build...
  • How soon before a trip should I put the patch on?
📖 Read our full Scopolamine Transdermal Patch guide →
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.

🧪 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 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII U725QWY32X
    Povidone K30 is a synthetic polymer made from petroleum. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in the stomach so the medicine can be absorbed.

2 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 DailyMedingredient 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.

💲 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 $8.13 $81.31 / 10 patch
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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Scopolamine 1 mg/3d 00378-6470-44 Mylan 24 patches $4.335 AB Availability likely
scopolamine 1 mg/3d 00591-2258-04 Actavis 4 patches $4.335 AB Availability likely
Scopolamine 1 mg/3d 42858-0150-14 Rhodes 10 patches $4.335 AB Availability likely
Scopolamine Transdermal System 1 mg 45802-0580-01 Padagis 1 patch $4.335 AB Discontinued
Scopolamine 1.5 mg 50742-0505-04 Ingenus 1 patch $4.335 AB Availability likely
Scopolamine 1 mg/3d 69238-1662-02 Amneal 10 patches $4.335 AB Availability likely
Scopolamine 1 mg/3d 70710-1846-02 Zydus 10 patches $4.335 AB Availability likely
Transderm Scop 1 mg/3d 10019-0008-01 Baxter 1 patch AB FDA listed
Scopolamine 1 mg/3d 50090-5349-00 A-S 4 pouches AB FDA listed
scopolamine 1 mg/3d 50090-7188-00 A-S 1 d AB FDA listed
Scopolamine Trandermal System 1 mg 63629-8450-01 Bryant 1 patch AB FDA listed
Scopolamine Trandermal System 1 mg 63629-8451-01 Bryant 1 patch AB FDA listed
Scopolamine Trandermal System 1 mg 63629-8452-01 Bryant 1 patch AB FDA listed
Scopolamine 1.5 mg 68071-3994-04 NuCare 1 patch AB FDA listed
Scopolamine 1 mg/3dthis 70771-1787-02 Zydus 10 patches AB FDA listed
Scopolamine Transdermal System 1 mg 71335-2718-01 Bryant 1 patch AB FDA listed
Scopolamine 1 mg/3d 71335-3013-01 Bryant 4 patches AB FDA listed
Scopolamine 1 mg/3d 71335-3014-01 Bryant 10 patches AB FDA listed
Scopolamine 1 mg/3d 71335-3015-01 Bryant 24 patches AB FDA listed
Scopolamine Trandermal System 1 mg 72162-1419-02 Bryant 1 patch AB FDA listed
Scopolamine 1 mg/3d 72162-2453-02 Bryant 4 patches 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

🏛️
2024
On the market since
Sep 2024
📍
2026
Currently FDA-listed
2 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.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Scopolamine — the program that covers self-administered drugs. 7 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 Scopolamine. 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
$7.24M
Claims incl. refills
112.6K
Beneficiaries
81.9K
Spend / beneficiary
$88.40
Spend / claim
$64.29
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
70771-1787-02 You're viewing this 10 POUCH in 1 CARTON (70771-1787-2) / 1 PATCH in 1 POUCH / 3 d in 1 PATCH 2024-09-05 Active
70771-1787-04 4 POUCH in 1 CARTON (70771-1787-4) / 1 PATCH in 1 POUCH (70771-1787-1) / 3 d in 1 PATCH 2024-09-05 Active
70771-1787-07 24 POUCH in 1 CARTON (70771-1787-7) / 1 PATCH in 1 POUCH / 3 d in 1 PATCH 2024-09-05 Active

Pack size FAQ

What quantity is in NDC 70771-1787-02?
NDC 70771-1787-02 is listed by the FDA — 10 pouch in 1 carton / 1 patch in 1 pouch / 3 d in 1 patch.
What NDC number is used to bill for this package of Scopolamine 1 mg/3d Patch, Extended Release?
Bill NDC 70771-1787-02 — the 11-digit billing format is 70771178702. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 FDA registers it as 70771-1787-2, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 70771-1787-02, written without dashes as 70771178702. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 70771-1787-02, the first segment (70771) is the labeler code FDA assigned to Zydus Lifesciences Limited; the middle segment (1787) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.
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 2 other package presentations of this same product, including 4 patches (70771-1787-04), 24 patches (70771-1787-07). 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.

📄 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 9 words

No readable label sections were found for this product.

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